Job Description
: We are seeking a detail-oriented and experienced Validation Contractor to join our manufacturing production team. This role is critical in supporting our production processes by reviewing and approving essential validation documents. The contractor will be responsible for drafting, redlining, and authoring Standard Operating Procedures (SOPs), as well as assisting in the preparation and execution of Installation Qualification (IQ) and Operational Qualification (OQ) processes. The ideal candidate will possess a strong background in validation within regulated environments, such as pharmaceuticals, biotechnology, or medical devices, and production manufacturing experience is a plus. This role will play a key part in ensuring that our production operations meet the highest standards of quality and compliance.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Required Skills & Experience
1. 1-5 years of experience in validation documentation within a regulated industry (pharmaceuticals, biotechnology, or medical devices).
2. Strong understanding of validation processes and regulatory requirements (e.g., FDA, EMA).
3. Bachelor’s degree in Life Sciences, Engineering, or a related field.
Nice to Have Skills & Experience
1. Background in training
2. GMP exposure
Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.