Compliance Specialist CMC, Quality Assurance Job at SGS Consulting, Massachusetts

dDZKV242eHpvQTNKTnVnOUoxK1duWGZvQ0E9PQ==
  • SGS Consulting
  • Massachusetts

Job Description

Job Responsibilities:

  • Essential Duties and Responsibilities include, but are not limited to, the following:
  • Performs QA review of executed GMP analytical batch records; in-process, release, and stability data to ensure compliance with regulatory requirements, internal quality standards, internal procedures, and contribute to the overall Quality Assurance processes.
  • Performs QA review of executed development studies intended for regulatory submissions, included but not limited to, draft batch records, analytical test records, and calibration records to ensure Developmental studies are conducted and data collected in compliance with approved protocols, appropriate corporate guidelines, internal procedures, domestic and global regulatory guidelines and standards.
  • Identifies and reports documentation errors and deviations from test / data records, protocols, Standard Operating Procedures (SOPs), or specifications in a timely manner.
  • Collaborates with cross-functional stakeholders regarding quality events, ensuring quality records are clearly written and technically sound with supporting evidence.

Skills:

  • Quality Assurance
  • Data Review
  • QA Review
  • GMP

Education/Experience:

  • BS/BA in Life Sciences, Engineering, or Chemistry, with 2-3 years of related Quality Assurance experience within GMP-regulated industry, or 1-2 years with Masters degree. In lieu of a Life Sciences degree, consideration will be given to candidates with minimum of 6+ years of industry experience in biotechnological and/or pharmaceutical quality, manufacturing, or other industry requiring high technical aptitude and attention to detail.
  • Working fluency in the Microsoft Office productivity suite (including Excel and PowerPoint).
  • Preferred Qualifications:
  • Demonstrated knowledge of cGMPs for biotechnology, cell therapy, and/or gene therapy and other international regulatory requirements.
  • Ability to interpret regulatory rules, guidance, and normative industry standards to make objective, risk-based decisions, and exercise sound Quality-by-Design principles.

Job Tags

Work at office

Similar Jobs

Estrem & Co.

Commercial Project Manager Job at Estrem & Co.

 ...Project Manager High-End Restaurant & Commercial Construction (Full-Time) - Miami, Florida Were hiring an experienced Project Manager to lead high-end restaurant and general commercial construction projects. This role is ideal for someone who enjoys fast-paced restaurant... 

Thermo Fisher Scientific

Medical Information Specialist - RN Job at Thermo Fisher Scientific

 ...improve health outcomes that people and communities depend on now and in the future. Location/Division Specific Information Within Medical Communications, we improve patient health by supplying medical information services to our customers, patients and healthcare... 

Winter

Ballet Teacher Job at Winter

Requirements:-Professional ballet teacher-Master degree or above Student age:18-23 Start to work:July/ August- Salary and benefits:- Salary 12k per month- Free apartment- Accident insurance- Paid summer and winter vacations Work load:- Mon to Fri

Bayer

Systems Reliability Engineer - 1st Shift (8am to 5pm Monday through Friday) On-Site Job at Bayer

At Bayer were visionaries, driven to solve the worlds toughest challenges and striving for a world where 'Health for all Hunger for none is no longer a dream, but a real possibility. Were doing it with energy, curiosity and sheer dedication, always learning from unique...

The TEA Center

Music/ Dance Teacher (Summer Camp 2026) Job at The TEA Center

Looking to be part of a growing successful child care center? As a Music teacher at the Transformational Education Adventure Center, you will be part of a fast paced business while making a difference in the lives of hundreds of children. - MUST Love working with children...