What are the responsibilities and job description for the Engineering - Assistant Process Engineer position at ECLARO?
Assistant Process Engineer
Job Number: 26-01754
Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for an Assistant Process Engineer for our client in Devens, MA.
ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
Position Overview:
If hired, you will enjoy the following ECLARO Benefits:
June Binuya
junethel.binuya@eclaro.com
2128047476
June Binuya | LinkedIn
Equal Opportunity Employer: ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.
Job Number: 26-01754
Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for an Assistant Process Engineer for our client in Devens, MA.
ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
Position Overview:
- The MSAT Process Engineering Contractor will support Manufacturing Science and Technology (MSAT) activities.
- There will be a focus on Out-of-Specification (OOS) investigations.
- Support OOS investigations; may take on investigation ownership as appropriate.
- Review batch records, process data, equipment logs, and analytical results to support investigation findings.
- Partner with Quality Assurance, Quality Control, Manufacturing, and Engineering teams to gather data and align on investigation scope and conclusions.
- Present investigation findings and technical rationale to cross-functional teams and management as required.
- Required Bachelor's degree in Chemical Engineering, Biochemical Engineering, Chemistry, or related technical discipline.
- Minimum 0-2 years of industry experience; cGMP or Cell Therapy manufacturing experience.
- Strong technical understanding of cell therapy manufacturing processes(Preferred)
- Technical writing skills for authoring impact assessments and out-of-specification investigations.
- Strong problem-solving, troubleshooting, and presentation skills.
- Familiarity with GMP documentation and electronic data systems.
- Ability to work collaboratively in a fast-paced environment.
- Strong analytical and critical-thinking skills with attention to detail.
- Effective communicator, able to work cross-functionally with Quality, Manufacturing, and Engineering stakeholders.
If hired, you will enjoy the following ECLARO Benefits:
- 401k Retirement Savings Plan administered by Merrill Lynch
- Commuter Check Pretax Commuter Benefits
- Eligibility to purchase Medical, Dental & Vision Insurance through ECLARO
June Binuya
junethel.binuya@eclaro.com
2128047476
June Binuya | LinkedIn
Equal Opportunity Employer: ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.
Salary : $30 - $32