What are the responsibilities and job description for the QC Analyst Microbiology position at BioSpace?
Job Title: QC Analyst Microbiology
Location:Framingham, MA
Shift: Sun-Wed 1200-2230
About The Job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
The Quality Control team is dedicated to the development and validation of is methodologies using state-of-the-art technology and responsible for ensuring that all production lots and materials meet the required quality standards, supporting regulatory compliance, and operational excellence of the organization.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve peoples lives. Were also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
About Sanofi
Werean R&D-driven, AI-powered biopharma company committed to improving peoples lives and delivering compelling growth. Our deep understanding of the immune system and innovative pipeline enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve peoples lives.
Main Responsibilities
Basic Qualifications:
#GD-SG
#vhd
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
Location:Framingham, MA
Shift: Sun-Wed 1200-2230
About The Job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
The Quality Control team is dedicated to the development and validation of is methodologies using state-of-the-art technology and responsible for ensuring that all production lots and materials meet the required quality standards, supporting regulatory compliance, and operational excellence of the organization.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve peoples lives. Were also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
About Sanofi
Werean R&D-driven, AI-powered biopharma company committed to improving peoples lives and delivering compelling growth. Our deep understanding of the immune system and innovative pipeline enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve peoples lives.
Main Responsibilities
- Executing analytical testing in a timely manner, ensuring adherence to the committed scheduled plans
- Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks
- Recording all expected raw data, calculations, information related to his/her tasks, to comply with cGMP and data integrity requirements
- Ensuring that he/she is trained and qualified to the assigned analytical testing that requires to be qualified
- Performing the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plans
- Informing his/her manager of any quality or HSE event (deviations, OOS,) in a timely manner to ensure investigation and impact assessment are performed appropriately
- Participating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately
- Executing assigned CAPAs related to remediation plans, continuous improvements
- Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately
- Ability to perform tasks in a Quality Control Laboratory environment and capable of lifting at least 10 pounds.
- May be required to pass vision exam to perform specific responsibilities.
- May be required to enter into controlled environments following proper gowning protocols
Basic Qualifications:
- High School Diploma or equivalent with a minimum of 4 Years of relevant industry experience.
- Associate Degree or Bachelors Degree with 0-2 Years of relevant industry experience.
- Proficient with Microsoft Office tools such as Word, Excel & PowerPoint.
- 1 Year of Experience in a GMP lab environment.
- Proficiency in Microsoft Office tools such as: Word, Excel & PowerPoint.
- Experience with lab-based data management systems.
- Experience in a Quality Control Laboratory.
- Experience with Environmental Monitoring, including Water Testing.
- Work in a laboratory with minimal use of chemicals.
- Ability to lift 10 lbs.
- Bring the miracles of science to life alongside a supportive, future-focused team.
- Discover endless opportunities to grow your talent and drive your career, whetheritsthrough a promotion or lateral move, at home or internationally.
- Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
- Takegood careof yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare,preventionand wellness programs and at least14 weeks gender-neutral parental leave.
#GD-SG
#vhd
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.