Scientist 1 - Flow Cytometry SME - 2nd Shift
Millipore Corporation

Work Location: Rockville, Maryland
Shift:
Department: LS-AS-TGCAD US OPS IMMUNO
Recruiter: Genie Hooper

This information is for internals only. Please do not share outside of the organization.

Your Role:

At MilliporeSigma, as the Scientist 1 - 2nd shift, your activities will support assay development through commercial application of new and innovative service offerings within the biosafety testing space. You are responsible for the scientific integrity of technical work performed in the laboratory, and are required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Requirements also include maintaining a thorough understanding of company testing services, technical principles and applications as they apply to your position.

• Shift hours: Monday - Friday 11am - 7:30pm
• Act as subject matter expert (SME) for specific defined area(s) of BioReliance business.
• For GLP studies, acts as Study Director.
• Fully responsible for the technical conduct of a GMP/GLP study, as well as for the interpretation, analysis, documentation, and reporting of results.
• Assure that appropriate technical specifications and standard operating procedures are followed.
• Assure that all experimental data, including observations of unanticipated test system responses are accurately recorded and reviewed.
• Assure that computerized systems used in the study have been validated or are under appropriate controls.
• Utilizes problem solving/ trouble shooting skills.
• Leads the completion of deviation investigation records in a timely manner.
• Liaise with Quality Assurance and appropriate cross-functional departmental areas to close the events and corrective actions identified during GxP laboratory testing.
• Maintains a working knowledge of lab procedures and assays.
• Creates/ revises SOPs, laboratory records and other related documentation as assigned.
• Writes technical reports for internal use and collaborates on papers for external use.
• Performs training of laboratory personnel as needed/ assigned.
• Contribute ideas and suggestions to improve standard laboratory techniques, protocols, processes, and equipment.
• Acts as key driver/ champion on project teams.
• Complies with company health and safety regulations and procedures.

Who You Are

Minimum Qualifications:

• Ph.D. in scientific discipline (Immunology, Chemistry, Biology, etc. ) with 1+ years of experience in a laboratory environment - OR -
• Master's degree in scientific discipline (i.e., Immunology, Chemistry, Biology, etc) with 3+ years of experience in a laboratory environment - OR -
• Bachelor's degree in scientific discipline (i.e., Immunology, Chemistry, Biology, etc) with 5+ years of experience in a laboratory environment

Preferred Qualifications:

• PhD in Immunology

• Extensive hands-on experience with Flow Cytometry/cell sorting techniques (potency, titer, viability or identity)
• Hands-on experience with Mammalian cell-based Immunoassays (preferred cell line, adherent cells e.g. HEK293; suspension T cell (SupT1, MT4, H9) and primary hematopoietic cells (CD34+ cells))
• Hands-on experience with Quantitative ELISA (Relative potency, titer, host cell protein, etc.)
• Experience with industry GxP compliance and Client facing experience
• Deviation investigation experience
• Intermediate skills in applicable computer programs (Softmax, PLA, or FACSDiva)
  Hand-on experience with equipment (FACSCanto, Cell sorters, Cell counter, Stemvision, automatic liquid handler, etc.)
• Excellent verbal and written communication skills that have been demonstrated through presentations/seminars, oversight of projects, implementation of new services, etc.
• Excellent time management skills, highly collaborative as well as independent and excellent multi-tasking abilities
• Demonstrates a high level of initiative and leadership capabilities.
• Effective coaching and training skills for complex and highly technical work
• Highly, technically competent

Pay Range for this position - $71,700 - $132,000

Our ranges are derived from several sources, and largely reliant on relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career level, and other job-related factors. This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k) matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses.

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

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