Analyst III, QC Raw Materials

Analyst III, QC Raw Materials

Location:

Canton, MA, US, 02021 Preparedness today, safer tomorrow. Emergent is a leading public health company that delivers protective and life-saving solutions to communities around the world. Here, you will join passionate professionals where our culture is informed by our values and commitment to protecting and saving lives.

JOB SUMMARY

Perform methods and procedures for inspecting, testing, and evaluating raw materials. Support program improvements including SOPs, new test methods, improved specifications, raw material qualification program, and alignment of raw material procurement with other Emergent sites. Streamline and improve compliance and efficiency in Quality Control programs and develop, implement, and maintain quality control systems and activities. Conduct out-of-specification and failure investigations, recommend, and implement corrective actions.

Responsible for generations, tracking, and completion of quality investigations and compliance records for the QC department.

ESSENTIAL FUNCTIONS

Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Supports the implementation of the raw material program ds change for revision of existing tests and identifies need for development of new assays in accordance with internal processes and consistent with compendial and GxP requirements, as applicable. Assesses compendial changes; leads change for revision of existing assays and identifies need for development of new assays in accordance with internal processes and consistent with compendial and GxP requirements, as applicable.

Perform daily activities in routine sampling raw materials, testing of raw materials and cleaning lab(weekly/monthly). Well versed in a wide variety of analytical and compendial methodologies and techniques such as FTIR, pH measurement, refractometry, density/specific gravity measurement using density meter, UV-VIS, distillation, titrations, AKTA, HPLC and GC. Perform entering sample and result of raw materials into Lims Lab Vantage system.

Communicate and coordinate with third parties and/or other departments. Prepares specifications, SOPs, and method verification protocols and reports. Ships samples and monitors test results produced by contract testing laboratories Communicates with raw material manufacturers to implement testing methodologies form daily activities in routine sampling raw materials, testing of raw materials and cleaning samples. Performs required data analysis, compiles data, and prepares results for review Conducts wet chemistry, chromatographic, and spectroscopic testing.

Performs other duties as assigned in support of QC Laboratory operations such as facilities qualification and routine monitoring testing, as well as QC testing, data reviews, sampling, and maintaining QC laboratory systems, when appropriately trained and qualified. Supports raw material testing equipment and instrument qualification, calibration, and preventive maintenance, as assigned. Lead Period Review, OOS, deviations, Change Control, and CAPAs;

designs and implements corrective action plans to address deficiencies. The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time which reflects management's assignment of essential functions.

MINIMUM EDUCATION, EXPERIENCE, SKILLS

Due to the nature of this role and our manufacturing environment, employees are required to meet certain health and safety requirements, including the ability to adhere to the Company's vaccination policies where job-related and consistent with applicable law. We are committed to providing a fair and inclusive hiring process and will evaluate reasonable accommodation requests for medical disabilities, or sincerely held religious beliefs, in accordance with applicable laws.

Bachelor's Degree in Chemistry or closely related scientific discipline with at least 5 years of relevant experience or Master's Degree with a minimum of 3 years of relevant experience. (Mainly QC Raw Material background) Experience with spectroscopic methods, chromatography, and wet chemistry methods. Familiarity with global pharmacopeias and monograph testing. Ability to follow SOPs and comply with cGMPs; generate SOPs.

Experience with implementing compendial test methods and performing a variety of analyses including computer-based instrumental analytics. Strong technical writing capability; can transfer ideas into scientifically sound and efficient study protocols and reports. Requires the ability to execute raw material assay methodologies including spectroscopy, wet chemistry, and chromatography. Experience working in a pharmaceutical testing environment. Requires good technical writing skills and the ability to effectively communicate with…