Qc Salary at Bomco Inc BETA

Job Description Job Description The Quality Control Technical Transfer Analyst III will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing, and stability studies when needed. Applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Responsibilities: Applies job skills and company's policies and procedures to complete a variety of tasks. Running test samples for In-Process, Lot Release, and Stability studies. Running test samples for (but not limited to) investigations, transfers, and validations. Reviewing assays Train

Senior Manager/Associate Director, Quality Control (QC) A Third Rock Ventures Stealth NewCo is seeking a Senior Manager/Associate Director, Quality Control (QC) to join their growing, experienced, and collaborative CMC team. In this role you will lead and independently perform technical and operational aspects of QC activities for antibody and fusion protein products across company’s pipeline. Successful candidates will be innovative, thrive in a startup environment and use their creative and imaginative problem-solving skills to help bring new products to patients. Key Responsibilities Develop strategies and execute QC activities for all pipeline programs, including in-process/release/stability testing, specification justification and maintenance, and critical documentation Oversee CDMOs for phase-appropriate analytical method development, qualification, validation, and transfer for in-process testing, drug substance (DS) and drug product (DP) release and stability testing. Review qua

job summary: Recommended Experience: Service now, Veeva, Trackwise, Active Directory, firewall rules, My Access, NTFS permissions. Excellent written and verbal communication. Applications impacted by upgrades, Idele candidate should have previous experience implementing, and or upgrading. Other application experience can be considered. Vaya Raman 7500 Fast PCR Hiac Particle Counters Maldi-tof Vi-Cell Cell counter Antaris II Waters Andrew + Alliance Working Environment: Must be able to work in controlled environments requiring special gowning. Will potentially be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body. No make-up, jewelry, contact lenses, nail polish or artificial fingernails, or any oral food, tabaco, candy etc. may be used in the QC / Manufacturing environment. During onboarding and training Onsite requirement will be 5 days per week. Afterwards minimum 3-4 days a week onsite is required. Must be able to work over

Onsite Expectations: For onboarding and training for the first few weeks should plan to be onsite 4-5 days a week. After onboarding and started working on projects, it is a minimum 3 days a week onsite, there will be times to be on site 4-5 days as needed. Job Description: The QC IT Application Analyst collaborates with the business and IT teams to provide project support for MA Biologics Operations Site Functions - Quality, Validation and Product Development. The QC IT Application Analyst manages their work with limited oversight- The scope of work includes, but is not limited to the following: Project upgrades from win 7- win 10 Provide oversight of vendor-provided solutions Handle ad-hoc technical requests from both internal and external partners in accordance with projects that are assigned. Work with other Direct team members for decisions, and clarification's as needed Must be able to juggle multiple projects and deliverables, and split billing time between projects where needed.

Job Description Job Description Title: QC Analyst III Duration: 1 year Location: Portsmouth, NH 03801 Pay Rate: $33.hr on W2 Key Accountabilities The Quality Control Technical Transfer Analyst 3 will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing and stability studies when needed. Applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Applies job skills and company's policies and procedures to complete a variety of tasks. Running test samples for In-Process, Lot Release and Stability studies. Running test samples

Scientist, QC, Data, Manufacturing, Technology

Job Description Job Description MICROBIOLOGY DX, BEDFORD, MA IS SEEKING A DIRECTOR OF MICROBIOLOGY. MICROBIOLGY DX IS A SPECIALTY MEDICAL LABORATORY. CERTIFIED BY C.L.I.A AND RECEIVES CULTURES AND SPECIMENS MAILED FROM ACROSS THE UNITED STATES AND THE WORLD. THE REQUIREMENTS ARE THE FOLLOWING: - A MASTER OF SCIENCE OR DOCTORATE DEGREE IN MICROBIOLOGY OR MEDICAL LABORATORY SCIENCE. - FIVE TO TEN YEARS OF HANDS-ON BENCH TESTING IN BACTERIOLOGY AND MYCOLOGY. - MUST HAVE KNOWLEDGE AND EXPERIENCE IN THE IDENTIFICATION OF BACTERIA BY BOTH WET CHEMICAL AND INSTRUMENTAL METHODS AND IDENTIFICATION OF MOLD AND YEAST BY MANUAL AND MICROSCOPIC METHOD. - EXPERIENCE WITH THE VITEK ANALYZER FOR BACTERIAL AND YEAST IDENTIFICATION AND ANTIBIOTIC SUSCEPTIBILITY TESTING. - MUST HAVE EXPERIENCE ANALYZING PROFICIENCY SPECIMENS FROM THE COLLEGE OF PATHOLOGIST PROFICIENCY PROGRAM IN BACTERIOLOGY AND MYCOLOGY. - MUST BE PREPARED FOR A HEAVY WORK LOAD. - MUST BE CAPABLE TO SPEAK WITH CLIENTS AND DOCTORS REGARD

Insight Global is looking for a QC Analytical Investigator to sit on-site at a brand new facility in the beautiful Seaport district of Boston supporting one of our top pharmaceutical clients. This is a first shift role, on-site Monday through Friday. This position will be supporting the growing technical services team in their risk assessment efforts. This role will be responsible for conducting RCA, assessing impacts, and developing CAPAs to ensure efficient and effective processes across the cell and gene therapy organization. A strong candidate for this role will have a strong background in QC Analytical risk assessments, in GMP environment, leading, writing and reviewing deviations and investigations. Th This person will need to be comfortable managing several projects simultaneously with various stakeholders, maintaining a project management mind-set. Additionally, they should be comfortable working independently and confidently managing decisions on their own. This is an amazing