What are the responsibilities and job description for the Senior Specialist, QC Analytical, Cell Therapy A2 Shift - Devens MA position at VetJobs?
Job Description
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.
Position Summary: Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. Perform method troubleshooting, training, and transfer/validation. Execute document
revisions, projects, deviations/investigations/CAPA, and continuous
improvement efforts.
Shift
A2: Sunday - Wednesday 2PM - 12AM
Key Responsibilities
Perform method transfer/validation and routine testing of in-process, final product, and stability samples.
Anticipate and perform routine troubleshooting and problem solving with minimal guidance.
Perform data verification, data review and review of GMP documentation for general and complex methods.
Perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
Train and mentor others on QC test methods, processes and procedures.
Perform other tasks as assigned.
Auto req ID
467106BR
Minimum Education Required
Masters
Job_Category
Health/Medical other
Additional Qualifications/Responsibilities
Qualifications & Experience
Specific Knowledge, Skills, Abilities
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
Demonstrated technical writing skills.
High problem-solving ability/mentality, technically adept and logical.
Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs.
Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
Advanced knowledge of LIMS, ELN and laboratory data analysis systems preferred.
Education/Experience/ Licenses/Certifications
Bachelor's degree or equivalent required, preferably in science. Netherlands: Bachelor's degree / HLO in (bioanalytical) science required.
4 years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
Demonstrated experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, ELISA, and aseptic technique).
Certificates/Security Clearances/Other
City*
Devens
State*
Massachusetts
Job Code
Pharmaceutical Pharmaceutical
Affiliate Sponsor
Bristol Myers Sqibb BMS
Salary Range
>$100,000
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.
Position Summary: Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. Perform method troubleshooting, training, and transfer/validation. Execute document
revisions, projects, deviations/investigations/CAPA, and continuous
improvement efforts.
Shift
A2: Sunday - Wednesday 2PM - 12AM
Key Responsibilities
Perform method transfer/validation and routine testing of in-process, final product, and stability samples.
Anticipate and perform routine troubleshooting and problem solving with minimal guidance.
Perform data verification, data review and review of GMP documentation for general and complex methods.
Perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
Train and mentor others on QC test methods, processes and procedures.
Perform other tasks as assigned.
Auto req ID
467106BR
Minimum Education Required
Masters
Job_Category
Health/Medical other
Additional Qualifications/Responsibilities
Qualifications & Experience
Specific Knowledge, Skills, Abilities
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
Demonstrated technical writing skills.
High problem-solving ability/mentality, technically adept and logical.
Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs.
Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
Advanced knowledge of LIMS, ELN and laboratory data analysis systems preferred.
Education/Experience/ Licenses/Certifications
Bachelor's degree or equivalent required, preferably in science. Netherlands: Bachelor's degree / HLO in (bioanalytical) science required.
4 years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
Demonstrated experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, ELISA, and aseptic technique).
Certificates/Security Clearances/Other
City*
Devens
State*
Massachusetts
Job Code
Pharmaceutical Pharmaceutical
Affiliate Sponsor
Bristol Myers Sqibb BMS
Salary Range
>$100,000
Salary : $100,000