Awarded the Deloitte Technology Fast 500 Award as one of the fastest growing companies in North America in 2010! Awarded by Deloitte Touche , Lannett is the fast-forward leader in the manufacture of generic pharmaceuticals as well as being a one-stop, blend to bottle manufacturer. We are seeking a highly talented and self- motivated professional to join our team as a QA Supervisor.
The successful candidate will develop into the Subject Matter Expert on QA Procedures, individual job functions in the QA Department and QA transactions in SAP. They will also meet departmental goals by leading and developing their assigned staff to meet and exceed safety, quality and productivity goals, among others in accordance with established policies.
Directly supervise assigned staff.
Interview and provide feedback on qualifications of candidates.
Train and develop assigned staff.
Plan, schedule and coordinate assigned staff and work load to ensure departmental goals are met.
Involvement in performance appraisals; rewarding and disciplining assigned staff.
Addressing and resolving complaints and problems.
Some Essential Duties and Responsibilities
Scheduling of assigned staff to ensure regular time and over time coverage.
Review and approve batch records.
Oversee Review and Release batch records, package orders and raw material records.
Supervise Inspection Lots to ensure timely sampling.
Supervise all QA Sampling Processes; i.e. raw materials, blends, finished goods.
Administer Cleaning Verification Reports issuance, tracking and approval.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Must be able to pass a company paid background check in order to handle controlled substances. Must have strong mathematical skills, and good cGMP knowledge. Must be detail oriented and must have proven technical writing ability.
Educational Requirements and/or Work Experience:
BS or BA in a related field or relevant work experience. 5 years supervisor experience and 10 years of work experience in pharmaceutical manufacturing. Some of those years must be in solid dose manufacturing. Read and write in English.
We offer a comprehensive benefits package, including medical, vision, dental, prescription, immediate eligibility in the 401 (k) plan with company match, Employee Stock Purchase Plan, and tuition reimbursement.
Please include your salary requirements in order to be considered. Candidates must possess authorization to work permanently in the United States. Seeking local candidates from the Philadelphia area only-no relocation provided. Lannett Company, Inc. is an equal Opportunity Employer.