Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.
Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.
Validation Consultant
Location: Durham, North CarolinaNote: Opportunity does not begin until May 2025, and it is short-term consulting.Provide computer system validation support for a leading contract development and manufacturing organization (CDMO) specializing in the production of biologics and advanced therapies. We are seeking a flexible and adaptable project management professional to represent our team in North Carolina. In this role, you will be responsible for the validation risk management, communication, an delivery.
Responsibilities
- Manage project plans and delivery for risk management in a large-scale Biopharmaceutical facility.
- Develop communication plans for risk management related to operations readiness.
- Conduct weekly meetings and deep dive sessions to monitor milestone objectives.
- Lead response and action plans for issues affecting on-time, high-quality operations readiness.
Skills and Experience
- Bachelor's degree in Engineering, Computer Science, or a related field.
- Minimum of 5 years of experience in CSV and validation within the pharmaceutical or biopharmaceutical industry.
- Strong expertise in validating project management in biopharmaceutical environments.
- In-depth knowledge of regulatory requirements (FDA, EMA, etc.) and industry standards (GAMP, 21 CFR Part 11) related to CSV and validation.
- Excellent problem-solving skills and the ability to analyze complex systems and processes.
- Ability to collaborate effectively with cross-functional teams.
- Proactive mindset with a strong attention to detail and the ability to prioritize tasks effectively.
- Experience working in a regulated GxP environment.
Joining Valspec as a Validation Project Consultant (CSV) will provide you with an opportunity to make a significant impact in the validation and CSV processes for cutting-edge life sciences manufacturing systems. If you are a highly motivated and detail-oriented professional with a passion for ensuring compliance and data integrity, we encourage you to apply.Benefits included.Valspec offers a standout culture, fantastic work environment, and has very competitive benefits to include premium medical, 401K match, profit sharing, tuition reimbursement, and other unique incentives.Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time.Any third-party unsolicited resume submission(s) will immediately become the property of Valspec.
Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.
