Quality Specialist II (Recombinant Proteins)

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 a fully onsite position based at our Cranbury NJ site. Unfortunately relocation assistance is NOT provided. Priority will be given to LOCAL candidates currently residing in Cranbury area.

• Must be legally authorized to work in the United States without sponsorship now or in the future.
• Must be able to pass a comprehensive background check which includes a drug screen.

Our Recombinant Proteins (REP) Business Unit in Cranbury NJ is part of our Biosciences Division. REP unites deep scientific expertise with a collaborative culture to build a product portfolio that includes cytokines growth factors antibodies and ELISA kits used to support the research of our academic government biotech and pharmaceutical customers.

We are seeking a highly motivated and meticulous Quality Systems Specialist to join our team. The Quality Systems Specialist will play a meaningful role in the implementation maintenance and improvement of the companys quality assurance program the Quality Management System (QMS) and ensuring that other departments operate in accordance with the highest quality standards and adhere to all applicable requirements. This position functions under the supervision of the Quality Manager.

What will you do:

• Maintain the companys QMS based on ISO 9001:2015 standard
• Conduct and assist with internal and external audits including Quality Management System audits
• Facilitate the identification investigation and effective closure of deviations non-conformances corrective and preventive actions (CAPAs) etc.
• Lead and manage root-cause investigations and facilitate problem-solving initiatives to implement effective corrective actions and drive process performance improvement (GMP OOSs NCRs DRs CAPAs and Change Controls)
• Coordinate in-house and external QC testing activities including sample submissions results analysis and reporting for WIP and finished goods. Tests include Biological Assays HPLC SDS-PAGE gels Endotoxin ELISA Protein Concentration by UV Spectroscopy Mass Spectrometry Western Blot Mycoplasma Sterility and Residual DNA testing
• Manage GMP finished product lot release and material disposition (Quarantine Hold Release Rework Scrap)
• Coordinate and implement GMP media fill challenges
• Review quality-related documentation such as manufacturing batch records worksheets and training forms for legibility accuracy and completeness
• Ensure the accuracy accessibility and version control of key company documents including SOPs work instructions test methods and checklists
• Perform daily tasks critical to seamless operation including material and product quarantine and release batch record and label issuance
• Manage product complaints and investigations and authorize replacements credits and refunds stemming from technical investigations
• Analyze quality data such as environmental monitoring and complaints to identify quality issues and recommend corrective and preventive actions for continuous improvement
• Establish and manage systems for collection and analysis of statistical data monitor and predict trends that may affect product quality
• Oversee site cleanroom integrity contamination control and state of control
• Complete and review quality questionnaires and desk audits
• Manage customer CDAs/NDAs
• Support maintenance of the Supplier Management Program
• Generate and disseminate change notifications customer notifications and product documentation (Certificates of Analysis Certificates of Origin Safety Data Sheets customer letters)
• Manage equipment maintenance programs with Facilities and maintain Quality Assurance-owned equipment
• Monitor and report on site quality metrics
• Collaborate with other departments to develop and maintain a robust QMS
• Follow all ISO 9001 and GMP guidelines
• Demonstrate and drive the Thermo Fisher values Integrity Intensity Involvement and Innovation (The Four Is)

Education:

• Advanced degree with at least 1 year of experience OR
• Bachelors degree with 3 years of experience OR
• Technical education equivalent to a 4-year college degree with 3 years of experience may be considered

Experience:

• Prior experience working in a controlled GMP environment is ideal
• Good understanding of ISO 9001 standard preferable

Knowledge Skills and Abilities:

• Preferred Fields of Study: Biology Chemistry Engineering Life Sciences or related scientific field
• Strong knowledge of cGMP regulations QMS ISO standards (9001/13485) and international regulatory requirements
• Experience with quality management systems and documentation (TrackWise OCPLM Master Control or equivalent)
• Experience in
• Proficiency in Microsoft Office Excel PowerBI
• Technical writing and documentation skills
• Analytical and problem-solving abilities
• Strong communication skills (written and verbal)
• Ability to work independently and without direct supervision
• Ability to work collaboratively in cross-functional teams
• Ability to create revise and interpret complex technical documents
• Consistently exhibits a high level of attention to detail
• Strong organizational skills including the ability to handle multiple projects prioritize and thrive in a fast-paced environment
• Ability to define problems collect data investigate and solve problems efficiently
• Proven track record of conducting presentations and trainings
• Experience conducting internal audits and supporting external regulatory inspections
• Project management and organizational skills
• Ability to work in cleanroom environments and follow gowning procedures where required
• Up to 10% travel may be required
• Physical requirements include standing/walking for extended periods and occasional lifting up to 25 lbs

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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