This position is a 2nd shift role, 1:30PM - 10:00PM. Supervise and perform regularly the preparation, formulation and dispensing of pharmaceutical products according to our current Good Manufacturing (cGMPs) and utilize Standard Operating Procedures (SOPs) in a clean room environment. Write and complete investigations, CAPAs, deviations and change controls utilizing root cause analysis tools and reporting software.
Area Of Responsibility
Supervise and perform the activities of technicians on the second shift in equipment and component preparation operations; dispensing API and excipients; formulation and filling and capping of parenteral drug products. Also responsible for overseeing the formulation and filling of dermatological drug products.
Schedule weekly plan of floor activities for technicians on second shift
Author and track to close investigations, CAPAS, deviations and change controls as required
Troubleshoot and solve moderate to complex problems related to the equipment, processes; existing or new products
Oversee inventory control in the production area and order supplies as needed for production to assure no delay in the manufacturing plan
Use systems like SAP, Track Wise, EDMS etc.
Evaluate team performance by conducting midyear and yearly reviews
Review completed batch records to ensure product is made in accordance with specifications
Review SOPs and Batch Records, and update through DCRs as needed
Work under limited supervision and follows clearly described procedures
Other duties as assigned
Education in Life sciences or technical discipline
Work Conditions:
Lab
Clean room/controlled classified areas
Manufacturing/production areas
Office
Exposure to noise
Exposure to Chemical/Biological hazards
Exposure to non-hazardous chemicals
Exposure to radiation within NRC limits
Exposure to/use of syringes and needles
Must wear scrubs/coveralls, safety glasses, safety shoes, gloves as required
Physical Requirements:
Stand, walk, sit, use hands and fingers to handle or feel, reach or push with hands and arms, stoop, kneel, crouch or crawl, climb, talk and hear
Able to operate lab equipment, production equipment and computer/office machines
Ability to wear Personal Protection Equipment
Lift up to 50 lbs.
Travel Estimate
Up to 0%
Education and Job Qualification
Bachelors degree in related field or equivalent experience
6 to 8 years of experience in pharmaceutical manufacturing
Excellent verbal, written and interpersonal communication skills
High level of initiative and self-motivation
Strong computer skills
Attention to detail
Ability to plan, prioritize and organize diversified workload
Team management skills
Record keeping skills
Safe chemical handling techniques
Knowledge of SAP, GMP, GDP, FDA, and OSHA regulations and standards
Experience
Minimum 2 - 5 years of supervisory or team lead experience
5 to 7 years of aseptic processing and aseptic area techniques experience
Experience with technical writing, root cause analysis and completing investigations, CAPAs, deviations and change controls
Numbers & Facts
Location
Billerica, MA
Skills
Active Pharmaceutical Ingredient (API)unmatched
Asepsisunmatched
Biologyunmatched
Biotech and Pharmaceuticalunmatched
Change Controlunmatched
Cleanroomunmatched
Communication Skillsunmatched
Computer Skillsunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Detail Orientedunmatched
Drug Manufacturingunmatched
Drug Productsunmatched
Establish Prioritiesunmatched
FDA Requirementsunmatched
GMP (Good Manufacturing Practices)unmatched
Identify Issuesunmatched
Interpersonal Skillsunmatched
Inventory Managementunmatched
Laboratory Equipmentunmatched
Leadershipunmatched
Lift/Move 50 Poundsunmatched
Manufacturingunmatched
OSHAunmatched
Office Equipmentunmatched
Order Suppliesunmatched
Presentation/Verbal Skillsunmatched
Problem Solving Skillsunmatched
Production Controlunmatched
Record Keepingunmatched
Root Cause Analysisunmatched
SAPunmatched
Standard Operating Procedures (SOP)unmatched
Team Lead/Managerunmatched
Technical Writingunmatched
Writing Skillsunmatched
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