What are the responsibilities and job description for the Equipment Validation Specialist III and IV (Pharmaceutical Manufacturing) position at SRG?
SRG, the leader in the Life Sciences human capital industry, is looking for a full-time, contract Equipment Validation Specialist III and IV to join our client's pharmaceutical manufacturing team in Portsmouth, NH.
*At this time we can only accept candidates for a W2 CONTRACT, we cannot accept C2C.
MUST HAVES:
- 6 (Level III) / 8 (Level IV) years of experience in validation in GMP setting
- 6 (Level III) / 8 (Level IV) years working with GMP equipment and systems
- Pharmaceutical industry experience required
JOB RESPONSIBILITIES:
- Ensures all critical GMP equipment and systems are validated and maintained in compliance with user requirements, process parameters and global regulatory guidelines.
- Provide Operations, Quality Assurance and regulatory bodies with scientifically sound, documented evidence that systems and processes will perform as required so they can be assured of a quality, compliant manufacturing environment.
** Only candidates selected to be moved forward in the recruitment process will be contacted by SRG's Recruitment Team to schedule a conversation.
Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.
If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.
Salary : $60 - $79
