Current jobs related to QC Supervisor - Verona - Randstad Life Sciences
-
Qc Analytical Chemist
3 weeks ago
Verona, United States Actalent Full timeJob DescriptionJob DescriptionJob Title: QC Analytical ChemistJob DescriptionJoin our Analytical Development Team within the Quality Control Department. The primary purpose of the QC Analytical Chemist 2 is to support the Production and Formulations Departments by analyzing pharmaceutical and cleaning samples using various procedures including internal...
-
Qc Analytical Chemist
1 week ago
Verona, United States Actalent Full timeJob DescriptionJob DescriptionJob Title: QC Analytical ChemistJob DescriptionJoin our Analytical Development Team within the Quality Control Department. This team collaborates with new clients to perform testing and method/validation transfers. We are currently in the early stages of partnering with a new client, where our raw material and finished product...
-
Quality Assurance Supervisor
1 day ago
Verona, Mississippi, United States Actalent Full timeJob Title:Quality Assurance SupervisorJob DescriptionWe are seeking a dynamic QA Supervisor to oversee the quality assurance process for our pharmaceutical and food products. In this role, you will ensure compliance and manage non-conformance issues related to raw materials and finished products. You will focus on assessing the release of products and...
-
Quality Assurance Supervisor
7 days ago
Verona, Mississippi, United States Actalent Full timeJob Title: Quality Assurance Supervisor - Pharmaceutical IndustryJob Summary: We are seeking a highly skilled Quality Assurance Supervisor to oversee the quality of our pharmaceutical products. The ideal candidate will have a strong background in GMP compliance and experience in managing a QA team.Responsibilities:* Ensure compliance with GMP regulations*...
-
Analytical Chemist
2 weeks ago
Verona, United States Actalent Full timeJob DescriptionJob DescriptionJob Title: QC Analytical ChemistJob DescriptionJoin our Analytical Development Team within the Quality Control Department. The primary purpose of the QC Analytical Chemist 2 is to support the Production and Formulations Departments by analyzing pharmaceutical and cleaning samples using various procedures including internal...
-
Entry Level Analytical Chemist
2 weeks ago
Verona, United States Actalent Full timeJob DescriptionJob DescriptionJob Title: QC Analytical ChemistJob DescriptionJoin our Analytical Development Team within the Quality Control Department. The primary purpose of the QC Analytical Chemist 2 is to support the Production and Formulations Departments by analyzing pharmaceutical and cleaning samples using various procedures including internal...
-
Lab Technician
1 week ago
Verona, Wisconsin, United States Actalent Full timeJob SummaryWe are seeking a highly motivated and detail-oriented Lab Technician to join our team at Actalent. As a Lab Technician, you will be responsible for maintaining a clean and organized laboratory environment, ensuring adherence to cGMP practices and policies, and assisting chemists and scientists with solution preparation and glassware cleaning.Key...
-
Lab Technician
3 weeks ago
Verona, United States Actalent Full timeJob DescriptionJob DescriptionLab Tech | Urgent Hire Essential Job Functions Cleans laboratory glassware and maintains the QC dishwashers. Replenishes storage locations as needed.Ensures adherence to CPI Standard Operating Procedures, analytical methods, protocols, company standards, and applicable regulations.Obtains purified water for the laboratory and...
-
Quality Assurance Manager
6 days ago
Verona, Mississippi, United States Actalent Full timeJob Title: Quality Assurance SupervisorJob Summary:We are seeking a highly skilled Quality Assurance Supervisor to oversee the quality control process and ensure compliance with regulatory requirements. The ideal candidate will have a strong background in quality assurance, excellent leadership skills, and the ability to make informed...
QC Supervisor
3 months ago
Job Title: QC Supervisor (Finished Product)
Duration: Direct Hire
Compensation: $75 to $90k (firm)
Shift: 1st shift, 8am to 4:30pm, M thru F
Position Overview:
The QC Supervisor – Finished Product (FP) will primarily assist Formulations, Supply Chain, Quality Assurance, and Production Departments by scheduling the analyses of pharmaceutical, dietary supplement, or food samples delivered to the QC laboratory. Support will be provided by ensuring that samples are analyzed using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendia monographs; client procedures; research procedures; and miscellaneous protocols. Sample analysis will mainly support commercial production or stability testing. The QC Supervisor - FP is expected to understand internal procedures and establish good laboratory practices. Additionally, the QC Supervisor - FP is expected to assist all Analytical Chemists and Scientists with method trouble shooting and compliance with all applicable procedures.
The QC Supervisor - FP will have a thorough understanding of USP, EP, ICH, and FDA guidelines as they relate to finished products, the required validations, and will lead laboratory investigations (i.e. quality investigations, out of specification investigations, etc.) as necessary.
The QC Supervisor – FP will serve as the supervisory lead on multiple projects, communicate regularly with clients, lead complex method validations / verifications. schedule staff on analytical testing, quote new projects, support monthly billing, and review and approve documents.
Essential Job Functions
- Mentors, trains, and supervises the Finished Product team. Additionally, QC Supervisor - FP will provide input and support to the Raw Material team as needed.
- Assists QC Management in the prioritization of workload and provides updates both internally and externally.
- Communicates with direct reports, management, co-workers, clients, contract laboratories, and vendors to coordinate all analytical finished product team activities such as quoting, testing, documentation, investigations, shipping, and billing.
- Drafts, reviews, and approves: SOPs, analytical methods, material specifications, deviations, and/or out-of-specification investigations.
- Drafts, examines, and implements protocols and summary reports related to routine stability studies, method validations, method transfers, and/or method verifications.
- Creates Finished Product CoA’s, as needed, to assist with the release of in-process and commercial finished products.
- Reviews Annual Drug Product Review (ADPR) documents submitted by QA for accuracy.
- Oversees testing involving dissolution, HPLC, GC, UV analysis, and various wet chemistry procedures.
- Assists all levels of Analytical Chemists and Scientists with tasks, questions, and troubleshooting of methods and/or instruments.
- Participates in on-site client and/or regulatory audits.
- Participates in contract lab qualification audits.
- Maintains awareness of changing regulatory and industry requirements (i.e. USP, FCC, EU, etc.).
- Generates and reviews QC metrics.
- Performs data review of laboratory notebooks, and forms as needed.
- Assists in maintaining a clean, organized QC laboratory.
- Conducts annual performance reviews and regular meetings with direct reports.
- Follows all client cGMP and safety practices, policies, and procedures.
- Employees work with and/or are familiar with the GMP requirements for Food, Dietary Supplements, Pharmaceuticals, or other elements of each.
- Depending on the position, the employee will be aware of Halal and/or Kosher requirements.
- Other duties as assigned.
Education/Skills/Knowledge Required
- 5+ years of supervisory experience in a cGMP pharmaceutical environment or a or applicable cGMP environment. Advanced degree may be substituted for experience.
- Thorough knowledge and understanding in the use, methodology, and troubleshooting of QC analytical equipment (i.e. HPLC, GC, and/or dissolution apparatus) and method development.
- Proven demonstration of supervisory and leadership skills to successfully train, direct, and motivate QC personnel required.
- Advanced time management skills to complete assignments/projects in a timely manner with minimal supervision.
- Ability to establish and maintain effective working relationships with team members, co-workers, vendors, and/or clients.
