The Fountain Group is currently seeking a Supplier/Vendor Quality Assurance Manager for a prominent client of ours. This position is located in Groton, CT (Hybrid role). Details for the position are as follows:
Payrate: $50/hr W2
Job Title: Supplier/Vendor Quality Assurance Manager
Location: Groton, CT
Duration: 7 months contract.
Hybrid: Required Onsite 2-3 days per weeks, will need to be local to the Groton Site.
Support US and UK time zones.
Strictly GMPs for this role, not GCP
Hard Skills:
1. Vendor Quality Management Exp. in Pharma industry
2. cGMP, not GCP
3. Project management
4. MS Office
Plus Skill:
1. Relationship building
2. Negotiation
3. Auditing
4. SAP
Job Description:
You will be a proactive partner with the external supply business lines, clinical product development teams, maximizing the contribution of Global Quality Operations with our external contract vendors. You will be the Vendor Point of Contact responsible for the quality management of approximately 25 contract manufacturers, packager, contract test laboratories, and supply partners globally. As a Quality Manager, you will focus on developing relationships, independently negotiating, developing and communicating Pharmaceutical quality requirements with contract vendors. Your expertise provides quality system leadership to operational teams, drive process improvement, advancing new concepts and methodologies that will make Pharmaceutical ready to achieve new milestones and help patients worldwide.
Provide guidance, lead/co-lead projects, manage own time to meet objectives, plan resource requirements for projects across the Department. Contribute to Quality Assurance by undertaking a variety of roles or assignments to further develop internal processes and people. Assess the operations executed at the supplier for their adherence to regulatory requirements, Quality Agreement requirements and Pharmaceutical expectations. Conduct quality reviews and report on results or defined quality analytics to in-country Medical Management, Platform Lines and Regional Medical Quality group, as appropriate.
Provides project support with current Good Manufacturing Practices to clinical supply packaging operations. Provides guidance on procedures and training necessary to be in complete compliance with current GMPs.
BS Preferred
If you are interested in hearing more about the position please respond to this posting with your resume attached or contact me at 813 444 5839.
Please forward this email to any friends or colleagues as we do offer a Referral Bonus for any candidate who is hired and still gainfully employed after 30 days.
Payrate: $50/hr W2
Job Title: Supplier/Vendor Quality Assurance Manager
Location: Groton, CT
Duration: 7 months contract.
Hybrid: Required Onsite 2-3 days per weeks, will need to be local to the Groton Site.
Support US and UK time zones.
Strictly GMPs for this role, not GCP
Hard Skills:
1. Vendor Quality Management Exp. in Pharma industry
2. cGMP, not GCP
3. Project management
4. MS Office
Plus Skill:
1. Relationship building
2. Negotiation
3. Auditing
4. SAP
Job Description:
You will be a proactive partner with the external supply business lines, clinical product development teams, maximizing the contribution of Global Quality Operations with our external contract vendors. You will be the Vendor Point of Contact responsible for the quality management of approximately 25 contract manufacturers, packager, contract test laboratories, and supply partners globally. As a Quality Manager, you will focus on developing relationships, independently negotiating, developing and communicating Pharmaceutical quality requirements with contract vendors. Your expertise provides quality system leadership to operational teams, drive process improvement, advancing new concepts and methodologies that will make Pharmaceutical ready to achieve new milestones and help patients worldwide.
Provide guidance, lead/co-lead projects, manage own time to meet objectives, plan resource requirements for projects across the Department. Contribute to Quality Assurance by undertaking a variety of roles or assignments to further develop internal processes and people. Assess the operations executed at the supplier for their adherence to regulatory requirements, Quality Agreement requirements and Pharmaceutical expectations. Conduct quality reviews and report on results or defined quality analytics to in-country Medical Management, Platform Lines and Regional Medical Quality group, as appropriate.
Provides project support with current Good Manufacturing Practices to clinical supply packaging operations. Provides guidance on procedures and training necessary to be in complete compliance with current GMPs.
BS Preferred
- (open to 5 + years' experience in lieu of degree).
If you are interested in hearing more about the position please respond to this posting with your resume attached or contact me at 813 444 5839.
Please forward this email to any friends or colleagues as we do offer a Referral Bonus for any candidate who is hired and still gainfully employed after 30 days.