What are the responsibilities and job description for the Validation Engineer position at Lead Candidate?
GBI Biomanufacturing is expanding their team! Having recently announced the signing of their first commercial contract, they are looking for great people to join them on their journey.
If you’d like to join this full-service exceptional CDMO during this exciting growth period, and you want to play a key role in keeping the world healthy, this could be your next career move!
What
As Validation Engineer, you will play a crucial role in ensuring the quality, compliance, and efficiency of manufacturing processes and systems. Main responsibilities include:
You
Ideally candidates will possess a Bachelor’s degree in Engineering, Pharmacy, Chemistry, or a related scientific discipline. Prior experience in validation activities within a pharmaceutical, biotechnology, or CDMO environment is highly desirable.
Intrigued? Send your resume to apply@leadcandidate.com
Don’t meet all the requirements? Don’t sweat! We’re always looking for an excuse to discuss your next opportunity. You might just surprise yourself...
Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.
If you’d like to join this full-service exceptional CDMO during this exciting growth period, and you want to play a key role in keeping the world healthy, this could be your next career move!
What
As Validation Engineer, you will play a crucial role in ensuring the quality, compliance, and efficiency of manufacturing processes and systems. Main responsibilities include:
- Develop and execute validation protocols, including but not limited to process validation, equipment qualification, cleaning validation, and computer system validation.
- Collaborate with cross-functional teams, including Manufacturing, Quality Assurance, and Engineering, to ensure that validation activities are planned, executed, and completed according to project timelines and regulatory requirements.
- Perform risk assessments and develop validation plans based on regulatory guidelines and industry best practices.
- Author and review validation protocols, reports, and standard operating procedures (SOPs) to ensure accuracy, completeness, and compliance.
You
Ideally candidates will possess a Bachelor’s degree in Engineering, Pharmacy, Chemistry, or a related scientific discipline. Prior experience in validation activities within a pharmaceutical, biotechnology, or CDMO environment is highly desirable.
Intrigued? Send your resume to apply@leadcandidate.com
Don’t meet all the requirements? Don’t sweat! We’re always looking for an excuse to discuss your next opportunity. You might just surprise yourself...
Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.
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