Laboratory Technician Pharmaceutical Job Description Sample
Senior Pharmaceutical Technician
Senior Pharmaceutical Technician
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, specifically roller compaction equipment. 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.
Responsible for ensuring cGMP compliance and generally good housekeeping.
Responsible for collaborating with Senior Pharmaceutical Technician or Pharmaceutical Manufacturing Lead to request work orders be placed for processing rooms and equipment (Roller Compactors) within core group.
Ensures product is visually inspected to ensure quality requirements are thoroughly met.
Responsible for requesting work orders to be placed for processing rooms and equipment within core group.
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.
Ensure that the facility is kept "tour ready" at all times and people/material/flow/cleaning and zone concepts are maintained at all times.
Set up and tear down of equipment
The minimum level of total work-related experience required to perform the job's responsibility is:
High school diploma – five to seven years of experience with a minimum of three years in a Pharma or cGMP manufacturing environment.
Technical degree/certification – three to five years of experience with a minimum of three years in a Pharma or cGMP manufacturing environment.
Previous experience with Roller Compaction technologies required.
Must have thorough equipment process and framework knowledge
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.
Thorough knowledge of Solid Dosage manufacturing preferred.
Excellent computer skills.
Must be able to manage priorities and projects prioritizing effectively.
Handling of raw materials for product assembly
Manipulation of drums to and from 6-inch pallets
Drum weight <10kg. (empty)="" to="" 150kg="" (max.="" full="" weight)="" multiple="" times="" per="">10kg.>
Maneuvering of drums in manufacturing area consisting of rolling, scooting, pushing and pulling (up to 80 lbs. of force)
Utilization of scoops and other hand held implements
Lifting boxes and/or containers from waist to chest height
Loading product of various amounts of completion to counters and quality control devices
Overhead lift and reach (≤15 lbs.)
Handling of finished product
Manipulation of drums to and from 6-inch pallets (up to 80 lbs. of force)
Push and pull ingredient canisters
Cleaning of area and equipment
Utilizing hand held brushes, wands, hoses, and other cleaning utensils
Operating in various postures
Overhead reach, squatting, kneeling, and forward bending
Transport of materials to and from designated lab space
Successful applicants will display Catalent's standard leadership competencies:
Leads with Integrity and Respect
Demonstrates Business Acumen
Fosters Collaboration and Teamwork
Engages and Inspires
Coaches and Develops
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
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees 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. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
Catalent. More products. Better treatments. Reliably supplied. ™
Visit www.catalent.com/careers to explore career opportunities.
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, protected veteran status, sexual orientation or gender identity. 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.
This position would be responsible for performing routine analysis of drug product, calibrating equipment, documenting test results, and providing general lab support functions.
- Prepare raw material, in-process and finished product samples for analysis.
- Document incoming samples and log test results.
- Perform routine analysis of drug product, including but not limited to wet chemistry analysis, analytical instrumentation and physical testing.
- All work performed within a cGMP lab environment supporting pharmaceutical production.
- BS in Chemistry, Biology, or related science.
- A positive attitude, willingness to learn and attention to detail.
Pharmaceutical Production Technician - Experienced
Join Bryllan where we offer our employees a full suite of benefits including health, dental, vision, life insurance, short and long term disability insurance, PTO and company match on our 401(k). In exchange, we are seeking colleagues at all levels who are focused on providing excellent customer service - internally and externally and who thrive in an entrepreneurial environment.
Bryllan LLC is a privately owned, rapidly growing Contract Manufacturing Organization (CMO) that has designed a unique sterile filling and containment platform for multi-product filling of cytotoxic, potent, live virus and vaccine, and hormone drug products. We offer a rewarding work environment while maintaining a small company, employee-focused atmosphere. Bryllan differentiates itself from our competitors by living our values of Integrity, Quality and Service.
We are currently seeking experienced pharmaceutical production technicians to join our operations team. Technicians will be responsible for all aspects of production, including dispensing, formulation, aseptic filling and packaging of our customers' product.
Successful candidates exhibit a strong knowledge of cGMP, desire to work in a team environment, seek opportunities for continuous improvement, and perform to the highest ethical standards. They may be required to lift up to 50 pounds, stand for long periods of time and wear appropriate PPE including proper gowning for entry into controlled areas. Applicants should also possess at least 6 years in a related environment through a combination of education and work experience (BS + 2 yrs. experience | Associates + 4 yrs. | HS + 6 yrs.)
All members of our Operations teams are expected to follow detailed SOP's and MBR's; maintain clean, safe and efficient work environments; comply with all regulatory and company specific safety and quality regulations; troubleshoot basic mechanical operations and equipment; operate and navigate equipment functionality through routine interaction with Human-Machine Interface or Supervisory Control and Data Acquisition systems; complete and review appropriate production and batch documentation accurately and consistently; perform equipment change-overs and cleaning for manufacturing; utilize knowledge and experience to improve procedures and processes; collaborate in a team environment including treating everyone with respect and courtesy and freely sharing knowledge. Selected candidates must possess a functional understanding of cGMP's and the impact of deviation from controlled processes or procedures.
Production Technicians will specifically:
Verify identity and quantity of components/materials for use in manufacturing.
Initiate and monitor equipment cycles (CIP, SIP, Decontamination, etc.)
Record GMP data on controlled documentation accurately, precisely, contemporaneously.
Transport hazardous and non-hazardous materials into/out of manufacturing area.
Wash, sanitize, and utilize material carts / bins / totes.
Complete and maintain training records within expected timelines.
Load and un-load materials into and out of rapid transfer ports, isolators.
Additionally, we seek colleagues who have the ability to develop and communicate corrective and preventative actions for process deviations; understand abstract concepts such as sterility and contamination; possess strong mathematical and organizational skills; exude honesty, integrity and commitment to the highest legal and ethical standards; work with minimal supervision; demonstrate pride in their work and an uncompromising commitment to quality.
As Bryllan LLC continues to grow, we offer a unique opportunity for individuals to grow and develop along with us. Our culture promotes teamwork, accountability, respect, continuous improvement, development and open communication. We encourage the use of knowledge and experience to mentor others and identify ways to improve our processes.
This posting is specifically for candidates with experience in pharmaceutical manufacturing. If you have not worked in pharmaceutical manufacturing, we encourage you to share your interest by applying to our general posting Growing Pharmaceutical CMO for future opportunities.
Medical Laboratory Technician (Mlt/Mt) - Part-Time, Weekend Nights
St. David's Round Rock Medical Center is part of St. David's HealthCare, one of the largest health systems in Texas, which was recognized with a Malcolm Baldrige National Quality Award in 2014. With 171 beds, the hospital's comprehensive services include advanced cardiac care at the Heart Hospital of Austin at St. David's Round Rock—the first specialized cardiac facility in Williamson County—with the only Hybrid Operating Room (OR) in the county; as well as emergency services in a 24-hour emergency department, including advanced trauma care with a Level II Trauma Center; St. David's Urgent Care Round Rock; and St. David's Emergency Center in Cedar Park. St. David's Round Rock Medical Center is also known for providing advanced orthopedic and robotic services, among other complex specialties. In 2016, the hospital received the Distinguished Hospital Award for Clinical Excellence from Healthgrades and also earned a national distinction for patient safety from The Leapfrog Group.
The Medical Laboratory Technician is responsible for competently performing moderate and high complexity testing in the areas of Hematology, Chemistry, Coagulation, Immunohematology, Microbiology, Urinalysis and Serology. Analyzes, reviews, and reports test results and quality control results and takes remedial action when indicated. Ensures specimen integrity by adhering to the laboratory's procedures for specimen handling and processing. Adheres to departmental policies and procedures including departmental programs, quality control, performance improvement, and safety.
ESSENTIAL JOB RESPONSIBILITIES
Performs laboratory testing.
Competently performs moderate and high complexity testing in Hematology, Chemistry, Coagulation, Microbiology and Serology.
Follows laboratory procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient results.
Operates test systems proficiently.
Troubleshoots test systems and takes appropriate action according to predetermined protocols. Notifies appropriate Supervisory personnel.
Ensures quality of laboratory services.
Follows established policies and procedures for quality control performance and documentation.
Performs and documents scheduled and unscheduled preventive maintenance.
Identifies problems which may adversely affect test performance or reporting of test results and takes appropriate action including supervisor notification.
Follows all safety, infection control, and OSHA Blood Borne Pathogen guidelines.
Participates in departmental performance improvement programs.
Participates in the Laboratory continuing education program.
Participates in "Total Quality Management" initiative (i.e. Modular Training, Process Improvement Teams, etc.).
Utilizes Departmental resources in an efficient manner.
Demonstrates efficiently by performing procedures rapidly and determining priority.
Utilizes appropriate supplies with minimal waste.
Operates equipment to maximize efficiency and minimize down time.
Promotes customer relations within the organization and in the community.
Communicates with the laboratory staff and customers to promote quality guest relations.
Maintains and supports a service-oriented relationship with its customers.
Respects and maintains the confidentiality of information relative to customers.
Strives to maintain a positive work environment.
Creates a supportive climate by serving as a role model of guest relations behavior.
Communicates via written, verbal, face-to-face, telephone, and computer methods.
EDUCATION AND EXPERIENCE
Required: Associate degree in a clinical laboratory science from an accredited institution, including a U.S. military program to be completed no later than 6 months from the date of hire.
LICENSES AND CERTIFICATES
Preferred: Certified in the area of Clinical Laboratory Science by the American Society of Clinical Pathologists, National Certification Agency for Clinical Laboratory Personnel, or equivalent.
Laboratory Technician - Manufacturing - Quality Assurance (Qa)
NOW Hiring Heroes is recruiting for an experienced Manufacturing Laboratory Project Manager. for a 3-6 month project for a client in Jacksonville, FL. The main role of this position is to lead the reporting of analytical data acquired through product test and final reporting..
• Be in the office during normal business hours (M-F, 8 to 5) to maintain all GMP requirements and standards
• Project setup and entry in Liquid Planner as defined by the clients head engineer.
• Manage tests of product from start to finish with little to no supervision.
• Responsible for creating final reports for the project managers.
• Overall responsible of maintaining onsite laboratory to the highest of standards..
• Archiving and scan work-order folders.
• Review client reports to make sure that all components of the report are present.
• Ensure project documents are complete, current, and stored appropriately.
• Ensure that issues are resolved and/or escalated in a timely fashion.
• Other duties as assigned.
• If education requirement are not me you must have at leas 2-5 years of previous experience as a Laboratory Project Manager or Senior Laboratory Technician.
• Exceptional verbal and written communication skills.
• Highly independent, problem solver and confident in their abilities
• Very organized and well versed in new technology .
• Ability to use (or learn to use) Liquid Planner and other computer software.
• Ability to work under pressure and manage several projects simultaneously.
• Ability to communicate difficult/sensitive information tactfully.
Associate Laboratory Support Technician (Jp4650)
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: Pilot Plant
Duration: 3 years
3Key Consulting Inc. is recruiting for an Associate Laboratory Support Technician with 1+ years’ experience in chromatography, biotech process development or manufacturing in a pilot or large-scale environment for a global, CA-based, bio-pharmaceutical company.
The Associate Laboratory Support Technician supports the execution of cell culture, harvest and downstream purification process studies using pilot scale equipment including bioreactors, chromatography skids and filtration systems. Routine tasks include:
- Equipment preparation, operating chromatography and filtration systems, compounding media and buffer solutions, and sampling.
- Utilizes scientific principles in execution of experiments and analysis of experimental data.
- Carries out laboratory tasks per plan and procedure in a team environment.
- Documents data and process information in accordance to good documentation practices.
- Performs laboratory safety evaluations.
- Organizes and stocks laboratory supplies.
- Performs minor equipment maintenance. Executes process/equipment troubleshooting.
- Performs daily cleaning and sanitization of the laboratory.
- Performs in-process testing using laboratory analyzers.
- Chromatography Experience - At least 1 year of experience preferred.
- Biotech Process Development or Manufacturing experience.
- Large Scale processing, buffer prep or media prep experience.
Equipment set up, operating process equipment, buffer/media prep, equipment cleaning, sampling of in-process product pools and sample management in electronic sample management system.
- Bachelor’s degree in Engineering or Science and one year related experience
- Ability to work occasional evening and weekend work.
- Prior hands-on experience in pilot-scale or large-scale cell culture or downstream purification process development or manufacturing operation
- Experience with automated and computer-controlled biopharmaceutical process equipment
- Knowledge of process data compilation and analysis
- Demonstrated equipment troubleshooting skills
- Excellent problem-solving capabilities and attention to detail
- Experience of collaboration within and across functional areas and outstanding customer focus Excellent written and verbal communication skills.
Supplement additional workload on team.
Employee Value Proposition:
Amgen and specifically this team are committed to staff development. This role has prepared staff for future development into:
- Bench process development.
- Process engineering.
- Technology transfer.
- Clinical and commercial manufacturing.
- Supply chain and logistics.
- Plant Engineering.
- Project management.
A high-level candidate with a PhD would not fit well in this role.
Interview process will be a phone screen by hiring manager and possibly 1-2 other managers followed by a face-to-face interview with hiring manager and 1-2 other managers
We invite qualified candidates to send your resume to firstname.lastname@example.org. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com. You are also welcome to share this posting with anyone you think might be interested in applying for this role.
Providence is calling a (Per Diem, Night Shift) Laboratory Technician to Providence Little Company of Mary Medical Center in Torrance, CA.
In this position you will:
Work under the direction of the Laboratory Supervisor, and in their absence under the direction of the Clinical Laboratory Scientist (CLS), to provide technical, clerical and patient care support services.
Perform a variety of procedures including venipuncture, skin puncture, specimen collection, specimen processing and distribution and the operation and maintenance of automated instrumentation up to but not including the resulting of laboratory data.
Service is provided to patients of all age groups: premature infants, infants, pediatrics, adolescents, young, middle and older adults.
Non-technical duties include taking of supply inventories, stocking supplies, cleaning and maintaining work area, equipment and instrumentation.
Provide service in a safe and professional manner and works within the established policies and procedures of the Laboratory and the organization.
Required qualifications for this position include:
California Certified Phlebotomy Technician
Communication in English, both orally and in writing
Must meet the physical requirements of this job listed on the RU-91 form for Laboratory Technician
Preferred qualifications for this position include:
One year's experience as a Laboratory Technician in a hospital based clinical laboratory
One year's experience as a phlebotomist
Ability to work flexible shifts
About the hospital you will serve:
Providence Little Company of Mary Medical Center San Pedro is a 259-bed nonprofit hospital that has served the Harbor and greater South Bay communities since 1925. Our Medical Center offers a comprehensive array of medical and surgical services each distinguished by innovation, quality and excellence in its respective area. We received the CHART "Certificate of Excellence" for receiving superior or above average results across the majority of outcomes and process measures publicly reported by CHART. We ranked in the top 21 among more than 240 hospitals throughout the state compared by California Healthcare Foundation, and were the first location in the South Bay to carry the Gold Seal of Approval® from The Joint Commission for Primary Stroke Centers. As a member of Providence Health & Services, we are continually driven by the caring tradition of our heritage – the foundation of our Mission and core values – to embrace respect, compassion, justice, excellence and stewardship. Providence Health & Services today celebrates unprecedented growth, recognition for top quality health care, a vibrant employee culture where new ideas are encouraged and a drive to help the underprivileged - all with an eye toward the future.
Pharmaceutical Development Technician
The Pharmaceutical Development Technician assist in manufacturing of sterile biologic products for clinical supply operations. Role will be focused on formulation of drug substance and includes preparation of production room, equipment and supplies for operation, process cleaning, and assisting in formulation of final drug form before filling. Other responsibilities include preparation of equipment and components and sterilization, upkeep and cleaning of production area and inventory management.
Assist in the manufacture of pharmaceutical parenteral products for use in clinical studies. Operations are carried out in a cGMP compliant manner with strict adherence to OSHA safety requirements, SOP's and batch records.
Unit operations include but are not limited to parts washing, parts preparation & sterilization, buffer preparation, active formulation, integrity testing of equipment & product filters, visual inspection and general maintenance and cleaning of the manufacturing area.
Responsible for equipment setup and operation, batch execution including completion of associated batch documentation and equipment logs, equipment cleaning and equipment storage.
Entry of data into computer terminals when required.
Position may include handling of potent compounds.
Perform in accordance with specific instructions, all operations necessary for the operation and cleaning of equipment used for the above mentioned operations.
Alert supervisor of any irregularities in procedures or equipment operation.
Perform preventative maintenance as required.
Adheres to the established manufacturing schedule for all assigned batches from start to completion
A two year Associate Degree in Science related to Pharmaceutical Development or equivalent field. In lieu of a two-year degree, a minimum of four years' working experience GMP pharmaceutical manufacturing or related field.
Proficiency in the use of computer programs/systems is essential.
Medical Laboratory Technician
Exciting opportunity to join the nation's largest provider of healthcare services!
HCA Healthcare is a national leader in providing modern, culturally competent, patient-centered care and we are driven by a single goal: the care and improvement of human life.
We are currently looking for an exceptional Medical Laboratory Technician to join our team. We believe in our team and your ability to help us provide high quality, compassionate care in the communities we serve.
We offer an excellent benefits package, competitive salary, tuition reimbursement, and growth opportunities. We are seeking a great addition to the team who feels patient care is as important as we do!
Interested in learning more about us? Click here!
Performs laboratory testing in the clinical laboratory.
JOB DUTIES INCLUDE BUT ARE NOT LIMITED TO
- Prepare samples for analysis
- Monitor tests and procedures
- Performs chemical analysis of blood and other body fluids to determine chemical components
- Mounts, stains, and examines smears under microscope for bacteria
- Performs hematological examinations making complete blood counts
- Examines smears for parasites or other irregularities in the specimen
- Performs other blood tests as ordered for patient care
- Performs a variety of bacteriological tests
- Performs quality control checks of instruments, solutions, and test results against established standards
- Performs microscopic examinations of body cells to identify abnormalities
- Performs routine laboratory procedures such as preparing slides and culturing media
- Prepares reagents, stains, and other chemical solutions
- Inventories laboratory supplies, cleans equipment and work areas and disposes of contaminated materials
- Logs patient specimens and enters test results on forms
- Collects data, prepares reports, answers correspondence, and compiles statistics as directed
- Attends required meetings and participates in committees as requested
- Participates in professional development activities and maintains professional affiliations
- Maintains equipment
- Orders and stocks all supplies
- Perform other duties as required
- Must read and understand and adhere to all Physician Services policies and procedures
- Practice and adhere to the Code of Conduct and Mission and Values statements
Knowledge of current medical terminology
Skill in problem solving
Completion of License/Certification program
Must be certified in accordance to state regulations
Certification bodies include American Society of Clinical Pathologists (ASCP), National Certification Agency for Medical Laboratory Personnel (NCAMLP), or the American Medical Technologists (AMT)
We believe in going above and beyond, and feel that there is no nobler pursuit than that of caring for and improving human life. We hope you'll join us on our mission!
Quality Assurance (Qa) Laboratory Technician - Food Manufacturing
Company Name: Crossroad Farms Dairy
Position Type: Employee
FLSA Status: Non-Exempt
Participate in programs to sustain compliance with Kroger Manufacturing Food Safety and Quality requirements. Responsible for product tests, audits and calibrations. Perform all jobs safely, efficiently and accurately to maintain and improve the performance of the entire plant in the areas of SQR and our Customer 1st strategy. Provide leadership that embodies our 7 Kroger Manufacturing High Performance Work System principles. Demonstrate the company's core values of respect, honesty, integrity, diversity, inclusion and safety.
Essential Job Functions:
Perform required product tests, audits and calibrations to ensure food safety and ensure consistent quality.
Maintain accurate documentation.
Complete tasks on "If down, do" lists.
Complete safety observations as assigned.
Keep work area neat and clean.
Ability to work overtime.
Follow established programs, policies and practices to produce safe, quality foods that meet regulatory and company requirements.
Support the development, implementation, maintenance, and ongoing improvement of the SQF 2000 Systems.
Accountable to the Kroger Manufacturing Food Safety and Quality Principles.
Must be able to perform the essential functions of this position with or without reasonable accommodation.
Minimum Position Qualifications/Education:
Must be at least 18 years of age
High school diploma or GED
Basic math and computer skills
Strong oral and written communication skills
Desired Previous Job Experience/Education:
Associate degree in related field
Minimum of two years previous quality assurance lab experience
Knowledge of food safety programs, microbiological and sanitation concepts
Functional knowledge and use of Microsoft Office
Education Level: High School Diploma/ GED Required
Required Travel: None
Required Certifications/Licenses: None
Position Type: Full-Time
States: Illinois; Indiana; Ohio
Jobs at Kroger Manufacturing: Through quality products, strong individual commitments and team spirit, Kroger has been established as a leader in the manufacturing industry. Kroger Manufacturing provides career development programs aligned with aspirations in Engineering, Process Management, Information Systems, Quality Assurance, Operations Management, Human Resources, Finance and Procurement. Our work force programs provide technically challenging rotations with cross-functional teams, plants and locations to allow our Associates to learn from some of the brightest minds in the business. Experience and training combined with mentoring and guidance from plant sponsors prepare our Associates with the skills and leadership behaviors needed to achieve a successful career at Kroger.
Kroger Family of Companies employs nearly half a million associates who serve customers in 2,782 retail food stores under a variety of local banner names in 35 states. Our Family of Companies also operates 2,268 pharmacies, 274 fine jewelry stores, 1,489 supermarket fuel centers and 38 food production plants in the United States. Kroger is dedicated to our Purpose: to Feed the Human Spirit™ by serving America through food inspiration and uplift and creating #ZeroHungerZeroWaste communities by 2025. Careers with The Kroger Co. and our family of companies offer competitive wages, flexible schedules, benefits and room for advancement.
Posting Notes: IN || Indianapolis || 400 S. Shortridge Road || 46219 || Crossroad Farms Dairy || None || Administrative Assistant; Manufacturing; Quality Assurance || Employee || Non-Exempt || Full-Time || None
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