Manufacturing Scientist III, Chemistry (Onsite)

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

Location:

This is an onsite position in Bedford MA. Residency near the site is required no relocation assistance provided.

DESCRIPTION:
Join our team at Thermo Fisher Scientific as a Manufacturing Sciences Scientist III where youll contribute to global health through innovative process development and optimization. Youll provide technical leadership in technology transfer process validation and manufacturing support across our facilities. Working at the intersection of R&D and manufacturing youll collaborate with cross-functional teams to ensure successful execution of manufacturing processes while driving continuous improvement initiatives. Your expertise will be vital in resolving complex technical challenges conducting investigations and implementing solutions that maintain our high standards of quality and efficiency.

REQUIREMENTS:
Advanced Degree plus 5 years of experience or Bachelors Degree plus 8 years of experience in GMP-regulated pharmaceutical/biotech manufacturing
Preferred Fields of Study: Chemistry Biochemistry Biotechnology Chemical Engineering or related scientific field
Strong technical expertise in process development scale-up and technology transfer
Advanced understanding of polymerization chemistry

Proven ability to lead complex investigations and implement effective solutions
Experience with process validation and qualification activities
Expert knowledge of cGMP regulations and quality systems
Strong analytical and statistical analysis capabilities

Advanced project management and documentation skills
Excellent verbal and written communication skills
Ability to work collaboratively in a matrix environment
Proficiency with statistical analysis software and Microsoft Office suite
Experience mentoring colleagues and providing technical training
Strong problem-solving skills and attention to detail
Ability to support manufacturing operations as needed including occasional weekend/off-hours coverage
Travel between local sites up to 20% may be required

Compensation and Benefits

This position may also be eligible to receive a variable annual bonus based on company team and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on which includes:

• A choice of national medical and dental plans and a national vision plan including health incentive programs

• Employee assistance and family support programs including commuter benefits and tuition reimbursement

• At least 120 hours paid time off (PTO) 10 paid holidays annually paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave) accident and life insurance and short- and long-term disability in accordance with company policy

• Retirement and savings programs such as our competitive 401(k) U.S. retirement savings plan

• Employees Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits please visit: Experience:

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