Current jobs related to QA Specialist - Cambridge - Alphanumeric Systems Inc.
-
QA Specialist
2 months ago
Cambridge, United States Alphanumeric Systems Inc. Remote Work Freelance Full time $57 - $60Alphanumeric is hiring a QA SPECIALIST - Level 2 to work in Cambridge, MA with our client of 20 years committed to improving lives through medical and pharmaceutical advancements.We are seeking a highly skilled and experienced Senior QA Specialist to join our dynamic team. In this role, you will be responsible for overseeing the quality assurance process,...
-
Senior QA Specialist for Incoming Materials
12 hours ago
Cambridge, Massachusetts, United States Proclinical Staffing Full timeJob Title: Senior QA Specialist for Incoming MaterialsProclinical Staffing is seeking a highly skilled Senior QA Specialist for Incoming Materials to join our team. As a key member of our quality assurance team, you will play a critical role in ensuring the quality and compliance of materials procured by our organization.Key Responsibilities:Conduct thorough...
-
Incoming Materials, Senior QA Specialist
5 days ago
Cambridge, United States Proclinical Staffing Full timeIncoming Materials, Senior QA Specialist - Contract - Cambridge, MAProclinical is seeking an Incoming Material Senior QA Specialist. Primary Responsibilities:You will play a critical role in ensuring the quality and compliance of materials procured by our organization. Your primary responsibility will be to evaluate incoming materials to ensure they meet...
-
Incoming Materials, Senior QA Specialist
2 days ago
Cambridge, United States Proclinical Staffing Full timeIncoming Materials, Senior QA Specialist - Contract - Cambridge, MAProclinical is seeking an Incoming Material Senior QA Specialist. Primary Responsibilities:You will play a critical role in ensuring the quality and compliance of materials procured by our organization. Your primary responsibility will be to evaluate incoming materials to ensure they meet the...
-
Incoming Material Senior
2 days ago
cambridge, United States Randstad Life Sciences US Full timeIncoming Material Senior (QA) Specialist7 monthsCambridge, MAMax PR: $80.70 /hr DURATION: Through May 2025100% On SiteParking is the responsibility of CW. This is a good question for CW’s to ask in the interview. I know there are a few different parking structures but the one located at or close to 301 Binney is roughly $420 I believe for the...
-
Incoming Material Senior
2 days ago
Cambridge, United States Randstad Life Sciences US Full timeIncoming Material Senior (QA) Specialist7 monthsCambridge, MAMax PR: $80.70 /hr DURATION: Through May 2025100% On SiteParking is the responsibility of CW. This is a good question for CW’s to ask in the interview. I know there are a few different parking structures but the one located at or close to 301 Binney is roughly $420 I believe for the...
-
Incoming Material Senior
6 days ago
Cambridge, United States Synectics Inc Full timeJob DescriptionJob DescriptionDescription:As an Incoming Material Senior QA Specialist, you will play a critical role in ensuring the quality and compliance of materials procured by our organization. Evaluate incoming materials to ensure they meet the required standards and specifications. Collaborate closely with procurement, manufacturing, quality control,...
-
Quality Assurance Specialist II
1 month ago
Cambridge, United States Randstad Life Sciences US Full timeExciting Pharmaceutical Company has a contract QA Specialist Position!Competitive Pay: Up to $61.63/HR W2. NO 1099 OR C2C optionTitle: QA SpecialistPosition type: This is a 1 year contract position with potential for extensionWork Hours: Monday-Friday 2nd shift 3pm-11:30PMLocation: Cambridge, MAJob Summary:We are seeking a highly skilled and experienced...
-
Quality Assurance Specialist II
1 month ago
Cambridge, United States Randstad Life Sciences US Full timeExciting Pharmaceutical Company has a contract QA Specialist Position!Competitive Pay: Up to $61.63/HR W2. NO 1099 OR C2C optionTitle: QA SpecialistPosition type: This is a 1 year contract position with potential for extensionWork Hours: Monday-Friday 2nd shift 3pm-11:30PMLocation: Cambridge, MAJob Summary:We are seeking a highly skilled and experienced...
-
GCP Quality Assurance Specialist
5 days ago
Cambridge, Massachusetts, United States Stratacuity: Proven Scientific Placement Full timeJob Title: GCP Quality Assurance SpecialistLocation: Cambridge, MA (Hybrid)Job Overview: Stratacuity is seeking a GCP Quality Assurance Specialist to oversee compliance and quality processes for clinical trials, managing relationships with CROs, Investigator Sites, and stakeholders.Key Responsibilities:Develop and maintain GCP Quality Systems and SOPs to...
-
GCP Quality Assurance Specialist
16 hours ago
Cambridge, Massachusetts, United States Stratacuity: Proven Scientific Placement Full timeJob OverviewStratacuity is seeking a highly skilled GCP Quality Assurance Specialist to oversee compliance and quality processes for clinical trials. As a key member of our team, you will manage relationships with CROs, Investigator Sites, and stakeholders to ensure seamless project execution.Key ResponsibilitiesDevelop and maintain GCP Quality Systems and...
-
GCP Quality Assurance Specialist
1 week ago
Cambridge, Massachusetts, United States Stratacuity: Proven Scientific Placement Full timeJob Overview: Stratacuity is seeking a skilled GCP Quality Assurance Specialist to oversee compliance and quality processes for clinical trials. This role will manage relationships with CROs, Investigator Sites, and stakeholders, ensuring seamless project execution.Key Responsibilities:Develop and maintain GCP Quality Systems and SOPs to ensure regulatory...
-
GCP Quality Assurance Specialist
2 weeks ago
Cambridge, Massachusetts, United States Stratacuity: Proven Scientific Placement Full timeAbout the RoleWe are seeking a highly skilled GCP Quality Assurance Specialist to join our team at Stratacuity: Proven Scientific Placement. As a key member of our organization, you will be responsible for overseeing compliance and quality processes for clinical trials, managing relationships with Contract Research Organizations (CROs), Investigator Sites,...
-
Quality Assurance Specialist
4 days ago
Cambridge, Massachusetts, United States Yoh Full timeJob Title: Quality Assurance Specialist - Incoming MaterialsYoh is seeking a highly skilled Quality Assurance Specialist to join our team in Cambridge, MA. As a Quality Assurance Specialist, you will be responsible for ensuring the quality of incoming materials and ensuring compliance with regulatory requirements.Key Responsibilities:Conduct thorough reviews...
-
Quality Assurance Specialist
4 weeks ago
Cambridge, Massachusetts, United States Alphanumeric Systems Inc. Full timeAlphanumeric Systems Inc. is seeking a highly skilled and experienced Quality Assurance Specialist to join our dynamic team in Cambridge, MA. We partner with a leading client dedicated to improving lives through medical and pharmaceutical advancements. In this role, you will play a crucial part in ensuring that our products meet both local and global...
-
Incoming Material Quality Assurance Specialist
18 hours ago
Cambridge, Massachusetts, United States Randstad Life Sciences US Full timeJob Title: Incoming Material SeniorJoin our team at Randstad Life Sciences US as an Incoming Material Senior, where you will play a critical role in ensuring the quality and compliance of materials procured by our organization.About the Role:As an Incoming Material Senior, you will be responsible for evaluating incoming materials to ensure they meet the...
-
Quality Assurance Specialist
2 weeks ago
Cambridge, Massachusetts, United States Alphanumeric Systems Inc. Full timeJob DescriptionAlphanumeric Systems Inc. is seeking a highly skilled and experienced Senior Quality Assurance Specialist to join our dynamic team.Key Responsibilities:Quality Assurance Oversight: Ensure that our products meet both Local and Global quality standards by executing all activities following quality and regulatory standards and procedures.Quality...
-
Senior Registered Nurse
6 days ago
Cambridge, Massachusetts, United States Mass General Brigham Full timeJob Title: Senior Registered Nurse - Quality Assurance SpecialistMass General Brigham is seeking a highly skilled Senior Registered Nurse to join our Quality Assurance team. As a Senior Registered Nurse - Quality Assurance Specialist, you will play a critical role in ensuring the highest quality of care for our patients.Job Summary:The Senior Registered...
-
Senior Registered Nurse
5 days ago
Cambridge, Massachusetts, United States Mass General Brigham Full timeJob Title: Senior Registered Nurse - Quality Assurance SpecialistMass General Brigham is seeking a highly skilled and experienced Registered Nurse to join our team as a Senior Registered Nurse - Quality Assurance Specialist. This role will be responsible for coordinating clinical quality assurance activities, including the development and review of training...
-
Quality Assurance Supervisor
4 days ago
Cambridge, Massachusetts, United States Vericel Corporation Full timeJob Title: Quality Assurance SupervisorVericel Corporation, a leading biotech company, is seeking a highly skilled Quality Assurance Supervisor to join our team in Cambridge, MA. As a key member of our Quality Operations department, you will be responsible for leading a team of QA Specialists and ensuring the highest quality standards in our manufacturing...
QA Specialist
3 months ago
Alphanumeric is hiring a QA SPECIALIST to work **2nd shift** in Cambridge, MA with our client of 20 years committed to improving lives through medical and pharmaceutical advancements.
We are seeking a highly skilled and experienced Senior QA Specialist to join our dynamic team. In this role, you will be responsible for overseeing the quality assurance process, ensuring that our products meet both Local and Global quality standards.
**Responsibilities**:
- Execute all activities following quality and regulatory standards and procedures.
- Promote a quality mindset and quality excellence approach to all activities.
- Continue support of continuous improvement culture and industrial excellence methodologies.
- Support employees and respective departments in a manner which is clear in approach, communication, and action.
- Provide proactive communication to customers to ensure timely escalation and resolution of issues. Follow up on issues to ensure completion in a timely manner. Support cross functional communication in all manners.
- Support batch release of drug substance including compilation of documentation, as needed
- Perform review of the manufacturing batch records for completeness and compliance with cGMPs as per regulatory requirements and internal procedures.
- Provide on the floor support to Manufacturing
- Perform SAP transactions applicable to batch record review
- Working knowledge and/or ownership of the following quality systems: Change Control, CAPAs, Deviations, and Self inspection auditing, QA reporting and approval of GMP documentation.
- Support GMP compliance and inspection readiness within organization. Assist in coordination of work for the QA Operations team to facilitate timely release of product lots.
- Perform review in Blue Mountain Ram for calibration, work order activities
**Basic Qualifications**: We are looking for professionals with these required skills to achieve our goals:
- HS Diploma or equivalent and 8+ years of experience in a cGMP environment, OR associate degree and 6+ years of experience in a cGMP environment, OR bachelor's degree and 4+ years of experience in a cGMP environment.
- Previous experience working with quality systems having oversight of cGMP production operations including some or all of the following: batch release, SAP, batch record review
**Preferred Qualifications**:If you have the following characteristics, it would be a plus:
- Bachelor of Science or Bachelor of Arts degree in a scientific discipline.
- Demonstrated experience in regulatory inspection activities.
- Ability to work on multiple projects on a tight timeline.
- Ability to prioritize and the flexibility to adapt to changing priorities.
- Working knowledge of cGMPs and associated regulatory requirements for the manufacture, testing, and release of pharmaceutical/biopharmaceutical products for international markets.
- SAP knowledge
- Experience working successfully both independently and in a team environment.
- Strong verbal and written communication skills.
- Able to interact with peers, subordinate and senior personnel in multidisciplinary environment including engineering, facility operations, validation, production, and QC.
- Able to prioritize and decide appropriate course of actions.
- Root cause analysis experience preferred.
- Vaccines experience a plus.
**About Alphanumeric Systems Inc.**: