Scientist I

Discovery Life Sciences • Malden, MA

1d • $62,000 - $70,000 • Onsite

About The Position

About Discovery Life Sciences:

Discovery Life Sciences (Discovery) is a leading provider of highly
characterized human biospecimens and cellular starting materials to advance cell
and gene therapy and precision medicine programs for cancer, infectious disease,
and other complex conditions. We routinely manage hundreds of studies and
expertly test thousands of biospecimens simultaneously. Leading biopharma,
diagnostic and academic institutions trust us to quickly deliver high-quality
biospecimens and reliable, reproducible biomarker data, so they can outpace
their competition and push the leading edge of innovation using our Science at
your Service TM business model.

Position Summary:

The Scientist I position will be reporting to a Principal Scientist, the
position will perform non-clinical (invitro) drug metabolism and drug-drug
interaction studies such as metabolic stability, enzyme induction and
inhibition, reaction phenotyping and transporter-based interactions for
pharmaceutical clients in accordance with study protocol and company standard
operation procedures (SOPs). The responsibilities will also include equipment
set-up, calibration and operation; test article and solution preparation; data
collection; documentation (both written and electronic) in accordance with
operating procedures; technical problem-solving; performing preliminary data
analysis for review by the Study Director; reviewing result data for the report.

A Day in the Life of a Scientist I at Discovery Life Sciences:

Perform non-clinical ADME testing studies.
Complete data forms and solution worksheets.
Assist in cleaning and routine maintenance of the lab
Administer maintenance to machines in preparation on of the next day.

Requirements

• Bachelor’s degree in biology, chemistry, or related science.
• 1-3+ years of experience performing research work in a laboratory.
• Knowledge of cellular and molecular biology and/or biochemistry.
• Experience in cell culture and enzymology.
• Knowledge and experience in good laboratory practice (GLP).
• Strong organizational skills with the ability to multitask and prioritize assignments; Ability to work on multiple projects to meet predetermined deadlines.
• Experience in invitro drug metabolism and drug-drug interaction such as metabolic stability, enzyme induction and inhibition, reaction phenotyping and transporter-based interactions.
• Familiarity with LC/MS analytical instruments.
• Strong computer skills to include Microsoft M365 products such as Excel, Word, PowerPoint
• Demonstrated verbal and written communication skills

Responsibilities

• Plan and perform non-clinical ADME testing studies with the supervision of a Study Director in accordance with general project plans, standard operating procedures, timeliness and applicable company productivity standards.
• Responsible for developing knowledge and aligning knowledge of company standard operating procedures and federal regulations applicable to duties and responsibilities (GLP, OSHA, etc.).
• Responsible for initiating meetings (daily or as needed) with Study Directors to review and approve study data.
• Responsible for ensuring that data collection forms and/or solution worksheets are signed by a qualified reviewer prior to submission to the Study Director.
• Responsible for submitting a complete packet of signed laboratory notebooks and/or data sheets in chronological order according to study start and stop date.
• Administer the repair or maintenance of equipment and ensure documentation of routine maintenance or non-routine maintenance.
• Assists or directs routine clean-up and maintenance of the general laboratory facility.
• Participate in Studies Meeting presentations, including reviewing, critiquing and presenting relevant journal articles or an area of the Associate’s interest or expertise with approval from Supervisor.
• Assists Study Directors in performing research studies including researching information to develop new methods and procedures for testing, data acquisition, data analysis, writing sections of the journal article.
• Attend scientific staff meetings including the Studies meeting and other mandatory company operational and training meetings.
• Ensure compliance with all laws and regulations applicable to the Company and its operations.
• Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described

Benefits

• Competitive salary and benefits package options including medical, dental, vision, life, and disability which start on your first day of employment!
• 401(k) match program which starts on your first day of employment
• Time away from work (Generous vacation and paid time off, paid parental leave, paid family leave, etc.).
• Professional development opportunities and reimbursement for relevant certifications.
• Collaborative and inclusive work environment that values diversity.
• Team-building activities and social events.
• Employee Referral Program and Colleague Recognition Program

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 251-500 employees