Laboratory Technician Pharmaceutical Job Description Sample
Pharmaceutical Laboratory Technician
Pharmaceutical Laboratory TechnicianMalvern, Pennsylvania Apply with System One Type:Contract Category:Scientific & Clinical Job ID:124869 Date Posted:01/25/2018 Pharmaceutical Lab Tech - Chester County BioTechnology company is hiring for an experienced Lab Tech with Solutions experience. Job Description
Responsible for maintaining the lab areas in full GMP compliance.
Responsible for ordering and/or preparing all reagents/materials for performing procedures and maintaining adequate and accurate inventory of all components.
Verifies that all batch records, SOP’s and specifications are up to date and reflect the current procedure.
Must be able to work with large quantities of human serum/plasma and whole blood.
Through cross training, provides assistance in other operations as requested.
Assures that all operations are performed according to SOP’s and procedures and any deviations from procedure must be reported immediately to supervisor.
Provides documentation on training on the proper use of appropriate batch records, SOP’s and specifications. Assures that all batch records are accurately completed.
Maintains all work areas in a clean and orderly state. Assures that products are stored and segregated and clearly identified.
Disposes of damaged, rejected or residual components/products according to SOP’s.
Identifies quality problems and reports product complaints (both internal and external) to supervisor.
Assures that all equipment is safe and all safety procedures are followed. Assures that all equipment is properly maintained, calibrated and validated prior to use.
Follows all company environmental, health and safety policies, procedures and guidelines and conducts work in a safe manner.
- Other duties as assigned
BA/BS required in life sciences
Minimum 2 years’ experience in biotech industry Be familiar with some or all of the following equipment depending on the area working in:
Laminar flow hoods
Vacuum pumps Apply with System One
Pharmaceutical Manufacturing Technician
Piper Clinical is currently looking for a Manufacturing Technician in Montgomery County, MD to work for a cutting edge biotechnology company. Responsibilities for the Manufacturing Technician Include: · The individual will be responsible for daily maintenance of cell lines, media formulation, freezing and thawing of cell lines, preparation of cells for ascites production · Testing of cell lines · Requisition of laboratory supplies and equipment, maintenance of equipment · Perform tasks under both GMP and GLP conditions and to maintain laboratory documentation · Periodic contact with clients (both written and verbal) may be required Qualifications for the Manufacturing Technician Include:
Pharmaceutical Manufacturing Technician
POSITION SUMMARY The manufacturing technician is an integral part of the overall process required to convert human plasma to injectable protein therapies. The technician is responsible for the set-up, operation and cleaning of various types of process equipment utilized to separate, purify, fill, inspect and package the protein products manufactured by Grifols.
ESSENTIAL DUTIES & RESPONSIBILITIES may include the following. Other duties may be assigned. 1. Responsible for equipment setup and operation in a biologics processing environment for plasma derived pharmaceuticals. 2.
Strict adherence to procedures and practices according to FDA regulations. 3. Strong emphasis on documentation according to FDA
Pharmacy Technician - Pharmaceutical Services
Job Title: Pharmacy Technician | Pharmaceutical Services | Sheldon
: PHARMACEUTICAL SERVICES
Hours Per Shift: 8 hr
JOB SUMMARY Compounds and dispenses medical prescriptions; maintains drug inventory and stock control systems under the direct supervision of pharmacists to ensure clinical and administrative effectiveness. Assists pharmacists in compounding, preparing and dispensing medical prescriptions to the public after receiving information from clients, customers or patients according to written/faxed prescriptions.
Uses computers to enter, access or retrieve data; establishes and maintains patient profiles, including lists of medications taken by individual patients and all new prescription and/or refill requests. Maintains proper storage and security conditions for drugs; controls inventory stock level and timeline to ensure adequate supplies. Coordinates departmental quality assurance and other client-focused services with supervisory staff; creates and maintains a safe working environment and conditions that adhere to state laws and regulations.
QUALIFICATIONS Must be registered and maintain certification with the Iowa Board of Pharmacy. All pharmacy technicians and all individuals training to work as pharmacy techs are required to register with the Board by completing and submitting a new application for registration within 30 days of accepting employment as a certified pharmacy technician or technician trainee in an Iowa pharmacy.
Must be nationally certified by an accredited technician certification board. Currently accredited boards are the Pharmacy Technician Certification Board (PTCB ) and the National Healthcareer Association (NHA).- An individual enrolled in a technician training course or program, or an individual who has not previously worked as a pharmacy technician and who accepts technician employment in an Iowa pharmacy, must register as a pharmacy technician trainee within 30 days of starting technician training or employment. A technician trainee must become a nationally certified pharmacy technician within 12 months of starting technician employment or training.
A pharmacy technician trainee who does not complete national pharmacy technician certification before expiration of the pharmacy technician trainee registration, must discontinue working as a pharmacy technician. High School Graduate or GED. Mandatory annual education as required by the facility and as required by the Iowa Board of Pharmacy. Prior experience preferred but not required.
About Sanford Health: At Sanford Health, we are dedicated to the work of health and healing. Every day, we show that commitment by delivering the highest quality of care to the communities we serve.
We are leaders in health care and strive to provide patients across the region with convenient access to expert medical care, leading-edge technologies and world-class facilities. In addition to strong clinical care, we are also committed to research, education and community growth. We engage in medical research to not only discover innovative ways to provide care, but also cures for common diseases.
We continuously seek new ways to achieve our vision of improving the human condition here in your community, across the region and around the world. The entire team at Sanford Health recognizes the value of healthy families and communities. We continue to gain momentum and expand our reach.
Together, we can make a positive difference now, and in the future. Sanford is an EEO/AA Employer M/F/Disability/Vet. If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-877-243-1372 or send an email to email@example.com . In compliance with federal law requiring employers to verify new employees' U.S. employment eligibility, Sanford participates in E-Verify. To learn more click here for English Version at https://e-verify.uscis.gov/emp/media/resourcesContents/EverifyPosterEnglish.pdf or here for Spanish Version at https://e-verify.uscis.gov/emp/media/resourcesContents/EverifyPosterSpanish.pdf .
Req Number: req15859
Senior Pharmaceutical Technician
Job Description: Position Summary Catalent is a leading provider of advanced technologies and outsourced services for the pharmaceutical, biotechnology and consumer health industry. Catalent develops, manufactures and packages pharmaceutical and other products for customers in nearly 100 countries, employs approximately 8,000 employees at 30 facilities worldwide and generates more than $1.7 billion in annual revenue. Among its core offerings, develops and manufactures oral and sterile pharmaceuticals in nearly all major dosage forms, and offers proprietary technologies used in many well-known prescriptions and over-the-counter products. Catalent is also the largest contract packager of pharmaceuticals. At the direction of the Supervisor, the Senior Pharmaceutical Technician is responsible for performing efficient set up / tear down, manufacture and cleaning of all equipment and processes associated with manufacturing operations with moderate supervision. The Senior Pharmaceutical Technician is responsible for policies and procedures with an emphasis on regulatory related processes such as SOPs, cGMP and safety in compliance with the CFRs and meets the business needs of the organization. Facilitates professional training for specific operational disciplines. Candidate must have a high attention to detail, excellent organizational and documentation skills while ensuring compliance with GMPs and applicable SOPs. Candidate will drive right first time in all aspects of operational performance. The Role
Responsible for ensuring cGMP compliance and generally good housekeeping.
Responsible for requesting work orders to be placed for processing rooms and equipment within core group.
Ensures 5S standards are met and maintained.
Ensure that the facility is kept “tour ready” at all times and people/material/flow/cleaning and zone concepts are maintained at all times.
Ensures product is visually inspected to ensure quality requirements are thoroughly met.
Ensure communication / execution of quality system improvement ideas provided by team, and commit to maintaining effectiveness of quality system components relevant to process.
Ensures that the Operators are adhering to all Catalent safety procedures and identifying/communicating the necessary adjustments to address potential safety concerns. Will also ensure the proper use of PPE (Personal Protection Equipment)
Focuses on driving productivity improvements while maintaining high quality standards
Drives reductions in unplanned deviations and focuses on troubleshooting identified equipment malfunctions.
Senior Pharmaceutical Technician should have high ability to trouble shoot and repair. Partners with scientists and Pharmaceutical Manufacturing Lead on batch record template issues to ensure clarity and drive accuracy for processing.
Ensures that areas of control are processing under GMP conditions and applicable SOP’s are being strictly followed
Works collectively with Warehouse and Supply Chain and other necessary areas to ensure timelines are met and results achieved. Responsible for managing material movement with WHS personnel so material delivery to processing room occurs on time.
Supports customer requests as needed
Partner with operational management to standardize training in operations.
Works with functional management, develops specific training requirements focusing on operational specific tasks as well as continued emphasis of FDA cGMP, DEA and Health & Safety regulations, and general work skills as needed.
Cooperates with Pharmaceutical Manufacturing Leads in the development of instructional material.
Collaborates with other departments to ensure seamless communication is established and ongoing
Participates in site committees such as EHS, Employee engagement or Quality committees.
Perform other duties as needed. The Candidate
High school diploma required
With High school diploma - 5+ years of experience with a minimum of 3 years in a Pharma or cGMP manufacturing environment
With Technical degree/certification – 3+ years of experience in a Pharma or cGMP manufacturing environment.
Must have a minimum of advanced operator qualification per supervisor / manager specified equipment train(s). Must be basic on all equipment within work zone.
Must have a thorough knowledge of cGMP, FDA, MHRA and DEA guidelines and how to apply them effectively. Position Benefits
Medical, Dental, Vision and 401K are all offered from day one of employment + 19 days of paid time off annually
Potential for career growth within an expanding team
Defined career path and annual performance review and feedback process About Catalent Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help develop some of the nearly 200 products we launch each year or help supply over 7,000 products for patients around the world. Catalent is an exciting and growing international company where our professionals work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market, for the benefit of patients globally. Catalent. More products. Better treatments. Reliably supplied. ™Visit www.catalent.com/careers to explore career opportunities, or contact us at +1 877 503 9493. Catalent is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected veteran status. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email along with the job number and title to Jobs@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be routed to a recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Catalent offers rewarding opportunities to further your career – join the global drug development and delivery leader! You will help develop some of the nearly 200 products we launch each year or help supply some of the over 7,000 products for patients around the world. Our highly skilled, dedicated global team of over 9,500 is passionate about improving the health of patients by combining their personal expertise with advanced technologies to advance science and supply innovative new products of the highest quality to patients globally. Why Catalent?
Gain unparalleled experience by working on multiple products and technologies – we launch nearly 200 new products for our customers each year.
We have 20 global pharmaceutical Product Development teams on five continents, who are, at any given time, working on over 700 new products and hundreds of ongoing clinical trials.
Our products include some of the latest life-saving medicines as well as some of the most well-known consumer health brands used by families every day.
Catalent’s more than 30 global facilities on 5 continents manufacture over 70 billion doses of over 7,000 important medicines and consumer health products.
Nearly 1 in 20 doses of medicines taken around the world has been touched by the Catalent team.
We have +1,100 patents on many superior patient-preferred technologies used by all the top pharmaceutical, biologic and consumer health companies.
We established the Catalent Applied Drug Delivery Institute to drive collaboration and scientific exchange among industry professionals, academics and partners.
Many of our 1,400+ scientists are regularly published in top industry journals and present at top industry conferences to advance knowledge sharing and the development of better life-saving medicines. Catalent is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected veteran status. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email along with the job number and title to Jobs@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be routed to a recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Pharmaceutical Packaging Technician (1St Shift)
The Company: Our client is a global healthcare company. The Company offers health solutions through its prescription medicines, vaccines, biologic therapies and animal health products. It operates through four segments: Pharmaceutical, Animal Health, Healthcare Services and Alliances. The Company's Pharmaceutical segment includes human health pharmaceutical and vaccine products marketed either directly by the Company or through joint ventures. Human health pharmaceutical products consist of therapeutic and preventive agents, generally sold by prescription, for the treatment of human disorders. The Company sells its human health pharmaceutical products primarily to drug wholesalers and retailers, hospitals, government agencies and managed healthcare providers, such as health maintenance organizations, pharmacy benefit managers and other institutions. Vaccine products consist of preventive pediatric, adolescent and adult vaccines, primarily administered at physician offices.
Education:High School Diploma or equivalent required. Associates or Bachelor's degree in Science or Healthcare field preferred. Experience: 1+ years of pharmaceutical packaging experience
Qualifications: Employees must possess good communication skills-both written and verbal, dexterity, exhibit a high level of attention to detail and be proficient with Microsoft applications. They should be self motivated and able to work independently as well as in a team. They show strong analytical and problem solving skills and are comfortable to work in a deadline driven area with changing priorities.
Performs all tasks related to clinical packaging while following appropriate Merck health and safety guidelines (using personal protective equipment as required), respecting specialist current GMP’s for Investigational products, adhering to the work order instructions and SOPs. Insures that each component or bulk material used in the packaging of a product is properly identified, not expired, weighed (when appropriate), verified throughout processing and corresponds to the written information on the work order before proceeding to the next step. Verifies before use that equipment calibration date has not been exceeded. Signs and dates utilization charts and all critical packaging steps in the work order documentation. When necessary, countersigns as an independent observer. Performs quality verifications and equipment challenge tests. In addition carries out all the periodic quality inspections during the packaging process.
Pay Rate: $21.00 per hour
Drug and background screenings required
One of the unique aspects of On-Board is our ability to customize solutions with each of the complimentary business verticals to satisfy our partners goals including Total Solutions.
McKesson is in the business of better health and we touch the lives of patients in virtually every aspect of healthcare. It starts with the chain of events you initiate when you work with McKesson Pharmaceutical - a chain that extends across the country and results in millions of people getting more from their healthcare. As the leader in pharmaceutical distribution and supply chain management, McKesson Pharmaceutical delivers vital branded and generic pharmaceuticals, as well as over-the-counter products, to more than 40,000 customers in three primary segments: retail chains, independent retail pharmacies and institutional providers such as hospitals, health systems, integrated delivery networks and long-term care providers. We base our distribution excellence on electronic order processing, asset management tools, a commitment to Six Sigma methodology, order accuracy and supply chain safety. We work with our customers on solutions - including supply management technology, world-class marketing programs, managed care and repackaging products and services - that help them meet their business and quality goals. Our entire team works to ensure patients receive their medications efficiently and begin the process of healing. As the nation’s largest pharmaceutical distributor, US Pharmaceutical is committed to driving total pharmacy health for customers and ensuring that customers receive the right drug at the right time, every time. This commitment is underpinned by McKesson’s focus on providing customers with the industry’s highest product availability, intelligent ordering capabilities and unmatched service accuracy. Join our team of leaders to begin a rewarding career.
Position Description Supports the integrity of repackaged drugs by performing stability testing and other required testing in support of Quality Operations in compliance with cGMP and FDA regulations. Assist laboratory analyst and stability coordinator with glassware, data review and verification, tracking, organization, and basic laboratory test.
Minimum Requirements + 1 years laboratory technician experience
Attention to detail with excellentorganizational skills will be critical
Perform general housekeeping dutiesincluding but not limited to washing and maintain laboratory glassware,sweeping, dusting, and mopping of the laboratory as needed.
Computer literate with workingknowledge of Microsoft Office programs.
Effective communication skills andability to collaborate at all levels
Ability to work well independently aswell as part of collaborative team
Ability to order supplies and trackinventory
Must be open to flexible 4 day/10 hours per dayworkweek, Monday through Thursday; must also be open to adjusting shift andovertime as needed based on business requirements.
Additional Knowledge & Skills
Verify data entry into stabilitysoftware
File and track laboratory methods,stability reports, data packets, etc.
Understand requirements from SOPs andGMP, for labeling and buffer preparation.
Knowledge of GMP and OSHA regulations.
Perform physical testing to ensuretimely release of laboratory results.
Perform daily calibration andmaintenance for laboratory equipment.
- HSDiploma or equivalent experience
- GeneralOffice Demands, standing for extended lengths of time, and occasional lifting
Benefits & Company Statement McKesson believes superior performance – individual and team – that helps us drive innovations and solutions to promote better health should be recognized and rewarded. We provide a competitive compensation program to attract, retain and motivate a high-performance workforce, and it’s flexible enough to meet the different needs of our diverse employee population. We are in the business of better health and we touch the lives of patients in virtually every aspect of healthcare. We partner with payers, hospitals, physician offices, pharmacies, pharmaceutical companies and others across the spectrum of care to build healthier organizations that deliver better care to patients in every setting. But we can’t do it without you. Every single McKesson employee contributes to our mission—whatever your title, whatever your role, you act as a catalyst in a chain of events that helps millions of people all over the globe. Talented, compassionate people are the future of our company—and of healthcare. At McKesson, you’ll collaborate on the products and solutions that help us carry out our mission to improve lives and advance healthcare. Working here is your opportunity to shape an industry that’s vital to us all. McKesson is an equal opportunity and affirmative action employer – minorities/females/veterans/persons with disabilities. Qualified applicants will not be disqualified from consideration for employment based upon criminal history.
Agency Statement No agencies please
Job:Research and Development
Pharmaceutical Sanitization Technician
We are seeking a Pharmaceutical Sanitization Technician to be responsible for the cleaning, disinfecting, and maintenance of all clean rooms and equipment in cGMP manufacturing areas. Primary schedule will run Monday through Friday from 11:30am-8:00pm, though occasional variation to those hours may be required.
Cleans, sanitizes, and decontaminates the manufacturing and cell culture areas and equipment according to cGMP guidelines, SOPs, and any other pertinent policies and controls.
Maintains inventory of clean room garments for gowning.
Requests all necessary components and operating materials in order to ensure daily operations.
Maintains good communication with support departments in order to comply with all manufacturing needs.
Completes all required production documentation in a legible, error free, and timely manner following good documentation practices.
Attends all mandatory cGMP training meetings.
Ensures a safe work environment is maintained at all times. Brings equipment and facility issues to the attention of supervisor for resolution.
Writes work orders when necessary.
Cross trains as back-up for component preparation employees.
High School diploma or General Education Degree (GED), with 1-3 years of aseptic experience in cGMP industry, or equivalent combination of education and experience.
Must be organized and possess basic math skills with the strong abilities to troubleshoot and problem-solve.
Must be able to easily understand and follow complex documented procedures, such as SOPs, and work in a clean room environment according to cGMP procedures.
Must be self-motivated and able to work with minimal supervision both independently and in a team setting.
Must be able to exert 50-100 pounds of force occasionally and/or in excess of 20 pounds of force regularly to move and lift heavy objects.
Must possess good oral and written communication skills and proficiency with MS Office.
- Proven ability to succeed in a fast-paced, deadline-driven environment, with the availability to work overtime hours when needed. Physical
Must undergo a company-paid post offer/pre-employment physical examination (health surveillance clearance with general eye exam to confirm ability to read a minimum of font size 10 with or without correction) and receive clearance to work from the attending physician prior to starting employment. This physical examination will be an annual requirement thereafter.
Must also be able to: be medically cleared and be “fit tested” (with a clean shaven face) to wear a respirator; maneuver/transport compressed gasses. Starting annual salary range of $40,000-$45,000, commensurate with experience, plus a comprehensive benefit program. Please provide salary history and/or expectations at the time of application. Resumes without salary information will not be considered. ID: 2017-1041 External Company Name: Immunomedics, Inc. External Company URL: http://www.immunomedics.com
Pharmaceutical Lab Technician
- Investigating deviations, including EMCARs, relevant to area of responsibility.
- Ensuring the completion and accuracy of investigations.
- Assisting other departments as needed.
- Ensuring compliance to cGMPs.
- Bachelors in Science (Biology, Biochemistry, Chemistry, Engineer, Physics)
- 0-2 years working in cGMP regulated environment, preferably pharmaceuticals.
- Knowledge of cGMPs and FDA guidelines.
- A positive attitude, good work ethic, and willingness to take on increasing levels of responsibility.
We partner with Chicago's top employers and match them with top talent. We represent many of Chicago's most desirable employers in their hiring efforts. They turn to Momentum for our industry specific expertise and ability to match them with the industries best candidates. Our boutique approach has made us the fastest growing scientific staffing company in Chicago.
At Momentum, we work with you to develop a job search strategy that suits your unique aspirations and skills. Our recruiting approach sets us apart from other staffing agencies by gaining a greater degree of partnership with you - the candidate. We attribute our success as a company to the relationships we’ve fostered with our candidates and contractors.
Ready to be a part of the Momentum revolution? Good idea. Here are some of the top reasons to work with Momentum:
- Full Time Healthcare - When you work with Momentum you're eligible for the same healthcare packages we have. All of our healthcare plans are Affordable Care Act compliant, don't have waiting periods and avoid federal tax penalties. You’ll be able to choose between Gold, Silver and Bronze plans. Better yet, we cover 50% of the monthly premium. Why should you be treated like a second class employee just because you are a contractor? Crazy.
- Industry Expertise - All we do is science. Period. Our industry focus gives us a greater degree of insight into what you should expect your career decision. We're experts at getting your career to where you want it to go. We'll help you understand your career options and work with you to determine the path that suits you. Why would you want to work with an agency that only does science on the side?
- Permanent Results - Last year 94% of our contractors were converted to permanent employees. Pretty impressive huh? Getting you a permanent job is our priority as an agency. No other agency in the scientific space can boast such a high conversion rate.
- No Charge - With Momentum there are no hidden fees. We don't take any money out of your paycheck or charge a conversion fee. Our clients pay for what we do, not our employees.
- Consultative Approach - When you work with Momentum, we start by learning a lot about your career direction. Only then do we propose a path that will help you achieve your career goals. We share a lot of our industry expertise with you so that you are informed about your options.
Our lead investigational therapy, sodium zirconium cyclosilicate, (ZS-9) is a novel agent for the treatment of Hyperkalemia, a potentially life-threatening condition characterized by abnormally high levels of potassium in the blood. As a member of the Quality Control (QC) team contribute through the completion of all assigned and routine laboratory related tasks in compliance with AZ, GMP & SHE standards. Key Accountabilities: · Ethical conduct and compliance · Provide support services for analysts and chemists in the quality control laboratory including cleaning and maintaining the general laboratory facilities and glassware, ordering laboratory chemicals and supplies, and inventory management · Perform sampling of raw materials, purified water, and compressed air for testing. · Accurately complete all data entry requirements for methods or tasks performed and reviewing data for completeness and accuracy. · Prepare solutions and standards per Procedures, Analytical Procedures and/or SOPs, with appropriate documentation · Clean and maintain the general laboratory facilities and notify appropriate maintenance personnel as needed · May fulfill other jobs/responsibilities as directed by management consistent with skill level and training. Essential
· Bachelor or Associates Degree, preferably in the chemical or biological sciences with previous experience in a pharmaceutical laboratory · Must be able to perform activities to support QC sampling activities including moving raw material drums, operating pallet jacks, and working in areas with limited access and on cat-walks around production equipment. · Must be able to retrieve, dispense, and dispose of chemicals and reagents according to according to approved procedures. · Must be adequately trained in Good Laboratory Practice (GLP and GMP) standards and be able to legibly and accurately complete all forms and/or notebooks. · Must be able to attain proficiency in using ZS Pharma analytical applications required for the completion of assigned tasks.
- Must be able to work at a lab bench or hood and perform the necessary procedures required for sample preparations and clean-up using the current prescribed or validated methodologies. ZS Pharma (an AstraZeneca group company) offers a salary and benefit package competitively placed within the local market.
We promote a culture where motivated, customer-oriented employees can flourish, experience professional fulfillment, and reach their highest potential. We offer medical, prescription, dental, vision, life and disability insurance plans, 401(k) with company match, paid time off (vacation, sick, holiday), Flexible Spending Account (FSA) and more. ZS Pharma Inc, an Equal Opportunity Employer
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