QA Supervisor Jobs in Pennsylvania

Job Title: 2nd Shift Quality Assurance Supervisor - Packaging (Locals ONLY) Company: Impax Laboratories, Inc Location: Philadelphia, PA Description: Implement & enforce policy directives which impact cGMP compliance in Philadelphia, packing facility Impax Laboratories, Inc. is a technology-based, specialty pharmaceutical company applying its formulation expertise and drug delivery technology to the development of controlled-release and specialty Generics in addition to the development of Branded products. Impax Laboratories, Inc. is headquartered in Hayward , CA , with additional locations in Pennsylvania and Jhunan Science Park , Taiwan , with both Domestic and International career opportunities available. Job Summary: The Quality Assurance Supervisor has the responsibility to implement and enforce those policy directives which impact cGMP compliance within the Philadelphia , PA packaging facility. The Quality Assurance Supervisor’s function is to administer certain programs directly (e.g., PMD approval process, protocol design for quality investigations) and to oversee and provide hands-on guidance to the Quality Assurance Inspectorate Group and Label Coordinators. This includes the monitoring of: sampling, the release process, line checks during packaging operations and label issuance and reconciliation. Direct Reports: The Quality Assurance Supervisor has responsibility for the Quality Assurance Inspectors (all grade levels), Junior QA Associates and Label Coordinators. Responsibilities: Oversee all aspects of product labeling to include reorders, revisions and the initiation of new labeling for review/approval through the system. Supervise the coordination of label material transfer activities to support line operations during a packaging run (includes inventory adjustments and packaging record execution). Supervise the activities of Quality Assurance Inspectors involved in the sampling and inspection of material receipts and line checks. Assign work schedules to staff based on operational activity and long range planning; monitor performance in meeting efficiency standards and conformance to cGMP compliance regulations. Supervise, train and evaluate personnel for adequacy in their positions and promote their professional development. Interact with Packaging Operations personnel regarding Quality Assurance/cGMP related issues. Initiate, review and/or approve various records and reports, e.g., label reorders, sampling/inspection results, batch records, Operational Variance Reports (OVRs), material reject reports, Inspection Protocols, vendor certification, and packaging specifications. Implement policy guidelines and initiate/approve SOPs. Participate in company-wide CI and quality circle initiatives and present cGMP compliance training programs. Assist in the performance of internal and vendor audits; detail corrective action and timely follow-up. Job Requirements: BA/BS degree in the sciences, although more extensive industrial pharmaceutical experience may substituted in lieu of degree. Eight to ten years experience in the pharmaceutical industry with at least 3 years in Quality Assurance. Supervisory experience necessary. Working knowledge of cGMPs. Ability to work independently to achieve results. Supervise and train the Quality Assurance Inspectorate staff. Self-starter with effective communication and leadership skills.

Job Title: Production Supervisor / Quality Assurance Leader Company: The Hunter Group Location: State College, PA Description: Our exclusive!  Global leader in the design and manufacture of niche electro-mechanical measurement products is seeking an early career lean manufacturing and quality assurance engineer to step into a newly defined hands-on shop floor management role.  This individual will lead tactical continuous improvement efforts at the plant level including supervising day-to-day activities of QA Engineers and Technicians, test scheduling, supplier qualification, and customer audits.  Must have recent hands-on engineering and shop floor experience, a can-do attitude and a results-oriented track record of quality assurance achievements.BS in Engineering or other technical degree is necessary.  ASQ certification a plus.  5+ years of experience, ideally with several years at team lead or supervisory level with emphasis on lean manufacturing and implementing continuous improvement initiatives.  US Citizenship or US Permanent Residency (Green Card) required.Located in a picturesque, family friendly region of PA.  Relocation assistance will be provided.Please send resume to:   Register to View

Job Title: Supervisor - Quality Assurance Company: Biotech / Pharmaceutical Company Location: West Chester, PA Description: Supervisor – Quality AssuranceLocation: West Chester, PA  OVERALL RESPONSIBILITIES:Responsible for the supervision of Quality Assurance employees and Quality Assurance Activities.  Areas of responsibility within Quality Assurance may include, but are not limited to, Document Control, CAPA, Complaint Handling, DHR Review, MRR Tracking, and Management Review Coordination.POSITION DUTIES & RESPONSIBILITIES:•    Supervise direct reports as assigned.•    Ensure Document Control, Complaint Handling, and other activities are performed in an accurate and timely manner.•    Ensure Device Master files are maintained (product drawings, process sheets, inspection sheets, etc.)•    Facilitate the Coordination of Management Review Meetings.•    Oversee the maintenance and administration of site CAPA system and SCAR system, if applicable.•    Performs other related duties as required.•    Know and follow all laws and policies that apply to ones job, and maintain the highest levels of professionalism, ethics and compliance at all times.•    Diligently participate in our compliance program-related activities as denoted by your supervisor or our Chief Compliance Officer.•    Promote and nurture the highest standards of professionalism, ethics and compliance, and actively support our compliance program-related initiatives and activities.•    Consistently enforce employee compliance, including attendance at training programs, and promptly report any non-compliance to the Chief Compliance Officer. PROFESSIONAL EXPERIENCE REQUIREMENTS:Minimum five years experience in the medical device or pharmaceutical industry.Minimum three years experience in Quality Assurance Systems such as Complaint Handling, CAPA and Document Control.EDUCATIONAL REQUIREMENTS:Bachelors Degree in Sciences, Engineering or other technical field.      OTHER REQUIREMENTS:Strong written and verbal communication skills.Strong organizational skills.

Job Title: Regional Quality Assurance Supervisor Company: DISH Network L.L.C. Location: Harrisburg, PA Description: Develop, implement and maintain quality assurance guidelines.Responsible for keeping local and regional installers up to date on the latest manufactures’ products and applications to achieve the highest quality installs.Responsible for reporting any safety violations and/or performance issues reguarding internal and external installations.Responsible for providing weekly and monthly reports to senior management.Ensures 100% satisfaction to customers.Train new and existing Quality Assurance Technicians, Field Service Managers, contractors and dealers to ensure quality and propler installation.Train for ensurance of all State, local and federal government guidelines and regulations.