Specialist, QA Quality Systems and Distribution (Senior)
This position is easy to learn and perfect for a first job. Specialist, QA Quality Systems And Distribution! This position offers a hybrid work model, combining remote work with time in our Remote office. This position requires a strong and diverse skillset in relevant areas to drive success. The salary for this position is set at a competitive salary. Â Â job summary:
As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and... biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!
location: Norwood, Massachusetts
job type: Contract
salary: $35.00 - 47.01 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
 Perform the release process confirmation for CMO batches, including Veeva documentation checks and SAP release steps.
 Conduct batch record review as needed
 Administration support for documentation archive in Veeva eQMS
 Ensure compliance with required training
 Resolve issues with CMO documentation in collaboration with CS leads and CMO leads
 Depending on skill set and previous experience, there may be need to rotate to support Compliance, operational excellence project work and/or quality project management teams.
qualifications:
 Sr. Specialist level (5+ years experience)
 Excellent communication skills
 Proficiency in regulatory requirements
 Familiarity in Veeva systems or similar quality document management
 Experience performing batch record review and batch disposition
 Familiarity in Drug Product GMP Manufacturing
skills: Quality Assurance, GMP (Good Manufacturing Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [email protected].
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
Applications accepted on ongoing basis until filled Apply Job! For more such jobs please click here! Don't Hesitate, Apply!Don't worry if you don't meet every single requirement. We value a great attitude and a willingness to learn above all. Submit your application today!
Apply Now
As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and... biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!
location: Norwood, Massachusetts
job type: Contract
salary: $35.00 - 47.01 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
 Perform the release process confirmation for CMO batches, including Veeva documentation checks and SAP release steps.
 Conduct batch record review as needed
 Administration support for documentation archive in Veeva eQMS
 Ensure compliance with required training
 Resolve issues with CMO documentation in collaboration with CS leads and CMO leads
 Depending on skill set and previous experience, there may be need to rotate to support Compliance, operational excellence project work and/or quality project management teams.
qualifications:
 Sr. Specialist level (5+ years experience)
 Excellent communication skills
 Proficiency in regulatory requirements
 Familiarity in Veeva systems or similar quality document management
 Experience performing batch record review and batch disposition
 Familiarity in Drug Product GMP Manufacturing
skills: Quality Assurance, GMP (Good Manufacturing Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [email protected].
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
Applications accepted on ongoing basis until filled Apply Job! For more such jobs please click here! Don't Hesitate, Apply!Don't worry if you don't meet every single requirement. We value a great attitude and a willingness to learn above all. Submit your application today!
Apply Now