Quality control scientist job description

Job Title: QC Scientist
Job Function: Performs Quality Control Method Transfer.
Job Type: Full Time Contract.
Location: Caguas, PR

About RCM:
RCM IT & Life Sciences is a leading provider of IT Business Solutions and Engineering Services to over 1,000 clients in the commercial and government sectors. RCM partners with clients to define implement and manage a broad range of technologies across multiple platforms, systems, and networks. Our broad geographic presence ensures that a proven and reliable tactical and strategic capability is available and deployable virtually everywhere in North America.

Scope of Job RCM is looking for QC Scientist to perform analytical method transfer in an FDA regulated environment for our client located in Caguas, PR.

Primary Responsibilities & Qualifications Experienced in method development, validation, and analytical technology transfer for API and finish good methods
Participate in the transfer of analytical technology to the commercial laboratories,
Perform testing of experimental, and registration lots, stabilities (CEDIPROF products) and new supplier certifications.
Interpret results obtained during method transfer and troubleshoot tests as needed.
Keeps track of the reagents and supplies inventory
Must be computer literate, bilingual (Spanish / English). Support EHS program to assure compliance with safety policies
Knowledge in FDA, USP and ICH guidelines for method development and validation
Bilingual (both English/Spanish).

Education & Certifications BS in Chemistry or related discipline and five years of related experience within the life sciences industry.

Equal Opportunity Statement

RCM is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Disclaimer

This job description is intended to describe the general nature and the level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. RCM reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.

Working as part of the QC Laboratory Operations Group, the QC Scientist routinely manages a number of assays pertaining to common techniques. Typically, the QC Scientist will be responsible for single projects (for one or several related techniques), may be part of a larger cross-sectional team leading small to medium multi-technique projects (as a molecule lead), or be part of a larger cross-sectional project working in conjunction with a more experienced QC Scientist or Lead Scientist.

Project requirements may include, but are not limited to; assay transfer, validation, sample analysis, batch/release testing, and stability studies. They will write protocols and reports, prepare and review analytical procedures, and be accountable for the approval and integrity of data and associated quality documentation.

The QC Scientist has knowledge within a relevant field and is able to troubleshoot techniques in the area of their expertise. The management and approval of assay data by the QC Scientist forms a large area of responsibility for GMP projects and therefore requires the ability to adapt to changing regulatory requirements, depending on project types.

In this role, the QC Scientist will provide internal customers with a central scientific point of contact for techniques within their area of expertise, or for external Clients where the QC Scientist is not the molecule lead. The individual is accountable for effective communication either directly with the Client or via the molecule lead to ensure that Client requirements and project deliverables are met. This includes discussion with the Project Management Office (PMO), molecule lead if applicable, and communication with QC Section Managers, as well as other scientific and analytical staff. The QC Scientist has scientific oversight of relevant techniques in order to ensure the successful initiation, planning, execution, monitoring and completion of projects.

The QC Scientist is required to have good working knowledge of GMP and regulatory guidelines as they ensure that projects are carrried out to the required standards, and that work is conducted in compliance with applicable regulatory requirements.

The QC Scientist will be responsible for overseeing the work of other QC Scientists where appropriate. They will be expected to train, coach and mentor members of the team and across functions as required.

The individual will work with more experienced QC Scientists or molecule leads to identify and communicate scientific and regulatory developments within their field of expertise, to include QA, management, Lead Scientists, QC Scientists and Laboratory Analysts. The QC Scientist may represent Labcorp internally or externally by preparing and/or giving presentations, writing or supporting the preparation of scientific papers and/or posters, in order to communicate the work of Labcorp QC laboratory operations.

The QC Scientist will be required to perform lab work as required, and provide support with regards to general laboratory operations and processes, leading by example to members of the QC operations team.

In support of project initiation and proposals, participate in conference calls and Client visits as required.
Perform and review gap analysis for Client methods being transferred in your area of expertise. Knowledge of the client requirements and plan accordingly to meet Client deadlines. Ensure Health and Safety information and risk assessments are in place and are readily accessible. Participate in and/or conduct project meetings. Attend client conference calls and meetings for specific technical requirements arising during projects. Work across all operational sections and other departments/sub-contractors associated with a specific project to achieve overall milestones. Prepare and approve project protocols and amendments. Ensure that the required regulatory, scientific and client requirements are captured. Perform content review of standard protocols for all assay types e.g. development, validation, sample analysis, release testing etc. Ensure assays are performed in accordance with the protocol, Client requirements and Labcorp Standard Operating Procedures (SOP). Complete test schedule (where appropriate). Coordinate or facilitate the scheduling or management of lab work, where necessary. Where appropriate, write or manage validated Analytical Procedures (AP) and Client Methods and competently review these documents. Perform lab work as required. Review and approval of non-regulated as well as regulatory GMP data. Write (where appropriate) assay based quality documents - Quality Events, Risk Assessments, CAPAs, Change Controls, Out of Specification (OOS). Perform tracking/trending and subsequent interpretation of assays and feedback to Operations and Clients as appropriate. When acting as molecule lead on more complex study types, review tracking and trending and feedback any potential issues to Operations and Client as appropriate. Identify and communicate adverse events to management and seek and find solutions to problems. Ability to problem solve unexpected analytical events within projects/assays, and issues within the wider group. Prepare project reports and Certificates of Analysis (CofA), and approve these documents where necessary. Accountable to address QA and Client comments on Protocols and Reports where necessary. Ability to make decisions on assay results/data. Write and approve assay investigation reports. Adhere to Quality Agreements and be aware of QC Scientist and Labcorp responsibilities.
Scientific Knowledge and Technical Expertise:
Technical expertise in one or more of the following scientific disciplines is desired:
Cell Culture and Cell-Based Potency Assays ELISA Statistics/Biostatistical experience pertaining to biopotency asays and/or In Vivo Relative Potency Assays. Virology qPCR Flow Cytometry
General Skills:
Computing skills, including word processing and use of spreadsheets (e.g. Microsoft Office packages and Microsoft Project). An in-depth understanding of health and safety policies, Company policies and procedures, and a good understanding of GMP. The post holder should be able to communicate effectively at all levels with other Labcorp employees, as well as external clients, suppliers, etc. The ability to get things done by influencing others (both internal and external). Knowledge of capabilities and expertise of the Labcorp organisation and companies that may provide support services. An up to date knowledge of regulatory guidelines. Commercial awareness, interpersonal and negotiating skills. Learn and maintain knowledge of process excellence processes, tools and activities. Experience will have been gained in similar types of study management (either internal or external). Experience with Client Management.
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Work at ROCKET PHARMA and help cure rare diseases!

Rocket Pharma is a fully integrated, clinical-stage company advancing gene therapies with curative potential for multiple rare childhood diseases. Rocket places enormous value on people and considers team member progress and well-being to be as important as the progress of its pipeline. We are looking for hands-on team players who enjoy collaborating with colleagues. We share a passion for seeking gene therapy cures for devastating diseases and making a difference for patients. This is an opportunity to become an integral part of a small, highly productive team and to help grow an entrepreneurial, scientifically driven organization that is increasingly recognized as a leading biotechnology innovator. In addition to a competitive compensation package featuring a generous 401K match and stock options, the position includes excellent health benefits.

Rocket Pharma is a company bringing hope and relief to patients with undertreated rare diseases through the development and commercialization of curative first-in-class gene therapies. We are seeking a Quality Control Scientist with experience in Immunochemistry to support the clinical manufacturing of a range of AAV and LVV Gene Therapy products.
Responsibilities:
Perform various Ligand Binding Assay Platforms.
Support daily QC operations of AAV products testing.
Qualify reference materials and critical reagents, prepare aliquots for storage.
Support testing of process development samples, method optimization/validation.
Maintain Cell line expansion for analytical use, prepare cell banking and cryopreservation.
Assist in planning and executing laboratory studies.
Author and review technical documents (protocols, reports, SOPs, test methods, memos and Impact Assessment).
Work with cross functional peers to meet company's deadlines.
Perform QC data review, generate CoAs and all related QC documents for QC release of products in accordance to Rocket's procedure.
Assure that all required QC records (testing, methods, protocols, reports and raw data) are generated and approved.
Train and assist junior QC associates in their functions.
Requirements:
MS in Biology, Biochemistry, Immunology with 6+ years of industry experience or BS in Biology, Immunology or Life Sciences with 10 years of relevant laboratory experience in Quality Control.
Knowledge of droplet digital PCR (dd PCR), qPCR.
Ability to work independently and make decisions.
Expertise in method validation.
Experience with mammalian cell culture.
Knowledge of FDA guidelines on method development/validation and/or ICH analytical procedures.
Expertise in analytical characterization of AAV and/ or other viral vectors is highly preferred.
Strong analytical skills to troubleshoot and investigate issues from the testing.
Expertise in multi color flow cytometry technology.
Ability to think critically and demonstrate problem solving skills.
Ability to interact, cooperate and motivate across departments and functions.
Ability to work independently while being a team player with collaborative skills.
Handle issues appropriately and with a sense of urgency.
Possesses a positive, can-do attitude and creatively solves problems
A diverse workforce fosters innovation and strengthens Rocket's business. We ensure equal opportunity without discrimination or harassment in the workplace on the basis of gender, race, color, religion, national origin, age, physical or mental disability, pregnancy, citizenship, status as a protected veteran, marital status, sexual orientation, gender identity and expression, genetic information, or any other characteristic protected by applicable local, state, and federal laws.

Full COVID-19 vaccination is required for employment at Rocket Pharmaceuticals.