Quality Control Scientist I - NMR

Tolmar Careers•Windsor, CO

1d•Onsite

About The Position

The Quality Control Scientist I - NMR is a technical leader within the QC functional area with a primary role in scientific development, testing and mentoring of junior analysts. The role is intended for a person with significant pharmaceutical laboratory experience who will contribute product specific scientific knowledge and analytical skills to the QC group. This position requires expert knowledge of NMR instrumentation and data analysis, fundamental chemistry pertaining to specific products and assays, analytical method validation, instrument qualification, and analytical testing of drug substances and formulations. The role also demands thorough knowledge of government regulations for drugs and medical devices, proficiency in various analytical instruments, and experience with cGMP practices and ICH guidelines. The scientist will be responsible for complex testing, troubleshooting, method development, and providing scientific recommendations to management and other departments. They will also participate in project teams, audits, and continuous improvement initiatives, ensuring adherence to all processes and procedures.

Requirements

Expert knowledge of NMR instrumentation and data analysis.
Demonstrated knowledge of fundamental chemistry pertaining to specific products and assays conducted in the Tolmar QC laboratory.
Strong sense of purpose and drive to meet deadlines without sacrificing quality.
Balances the need for speed with a commitment to accuracy and quality, completing tasks thoughtfully and effectively.
Knowledge in analytical method validation and instrument qualification.
Expert knowledge in analytical testing of drug substances and formulations for Chemistry or Microbiology.
Thorough knowledge of government regulations of drugs and medical devices as they apply to laboratory work.
Ability to grasp and enhance the technical expertise required for new products in the pipeline in order to support QC functions as per business needs.
High level of proficiency in Quality Control laboratory procedures and testing techniques.
Hands-on, operational and troubleshooting knowledge of analytical instrumentation within the QC department.
Ability to evaluate and adapt new technologies that are to be introduced to the department based on business needs.
Knowledge of analytical troubleshooting and product investigation.
Expert knowledge of cGMP practices, regulatory and ICH guidelines.
Excellent grasp on USP and other compendial methods.
Proficient in the use of analytical laboratory instruments such as HPLC, FTIR, GPC, GC, and UV-Vis spectrophotometers, CCIT, plate readers, and MODA.
Ability to prepare, review, conduct and assess analytical method validations, feasibility and suitable for use.
Knowledge of computer applications including Microsoft Office.
Experience in authoring technical reports.
Excellent oral and written communication skills demonstrated through interactions internally and externally.
Ability to manage multiple projects concurrently and under tight time constraints.
Previous in depth NMR testing and troubleshooting experience is required.
BS combined with 10 or more years Pharmaceutical cGMP laboratory work.
Masters combined with 8 or more years Pharmaceutical cGMP laboratory work.
PhD: and 5 or more years Pharmaceutical cGMP laboratory work.
Experience in the pharmaceutical industry to include experience with cGMP analytical testing of drug substances (DS) and Drug products (DP), preferably in high-volume Quality Control laboratory required.

Nice To Haves

BS, MS or PhD in Chemistry, Biochemistry, Pharmaceutical Sciences or related field.

Responsibilities

Assume a high level, in-depth scientific leadership and mentoring role in the QC laboratory for junior analysts and peers.
Conduct complex and challenging QC testing using a variety of instrumentation that needs a high level of analytical technical expertise and in-depth knowledge in chemistry.
Act as a primary technical resource for and be a point of contact for QC and external departments.
Resolve testing issues including Out of Specifications and investigations for commercial, stability and developmental samples.
Provide scientific recommendations and technical expertise for new instrumentation and methodology.
Make scientific recommendations to management and other departments regarding Quality Control laboratory protocols and test procedures.
Assist laboratory management in test assignments based on commercial and stability time lines and provide hands-on testing support during commercial exigencies.
Assist the departmental leadership in new endeavors including efficiency efforts, organizational tasks, and non-routine activities.
Assume a supporting role to the management team on activities such as the issuance of COAs, review of Change controls, test methods and specifications.
Provide support to the QC department for the evaluation and implementation of new technological innovations in laboratory automation systems, documentation systems and other technologies.
Perform change assessments and change controls for changes in testing, documents and specifications.
Validate and install new laboratory instrumentation systems including development of new test methods for the associated instrumentation.
Serve as a project team member and collaborate with CORE teams throughout the development lifecycle.
Prioritize workload to meet timelines while ensuring on-time delivery of all projects, testing and action items.
Take ownership of tasks and results from initiation to completion to meet commitments and proactively address outcomes.
Escalate and communicate items that arise per the timelines specified in the department escalation strategy.
Execute all business and department goals and initiatives on time.
Support and execute all potential 3-day field alert investigations and actions expeditiously.
Submit document change requests for all document updates and minimize document revisions for routine updates where possible.
Identify, and complete cost savings initiatives and facilitate continuous improvement.
Participate in leadership development activities and take an active role during department and company activities.
Participate on project teams, company and department meetings, third party audits, and regulatory audits.
Demonstrate leadership aptitude in technical functions.
Ability to perform designated duties under minimal supervision and support departmental management in all aspects of organizational functions.
Ensure adherence for compliance with all processes and procedures including training completions, QE and CAPA due dates, notebook and logbook audits, archiving, schedules, internal assessments.
Accountable for maintaining a positive atmosphere of teamwork, camaraderie and respect towards co-workers.
Participates in required annual hazardous waste training.
Respond to spills per CP 030-0202 Chemical Spill Response.
Perform various other duties as assigned.