Metrologist at Tris Pharma

South Brunswick, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

15 Jan, 26

Salary

0.0

Posted On

17 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Calibration, Instrument Performance Verification, Analytical Methods, Good Manufacturing Practices, Documentation, Problem-Solving, Communication, Team Collaboration, Time Management, Analytical Thinking, Laboratory Investigations, Regulatory Compliance, Microsoft Office, Laboratory Software, Color Identification, PPE Usage

Industry

Pharmaceutical Manufacturing

Description

Description Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned U.S. biopharmaceutical company with a focus on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. We have >150 US and International patents and market several branded ADHD products in the U.S. We also license our products in the US and ex-US markets. We have a robust pipeline of innovative products spanning neuroscience and other therapeutic categories employing our proprietary science and technology. Our science and technology make us unique, but our team members set us apart; they are the engine fueling Tris’ passion and innovation. Our colleagues understand the criticality of operating a successful business and take pride in the company’s success. Equally importance to each team member is how we interact with one another on a daily basis. We believe in each other and in respectful, open and honest communications to help support individual and team success. Our Metrology Department, located in our Monmouth Junction, NJ headquarters has an immediate need for a Metrologist. (Title/level and salary commensurate with experience and will be determined after the interview.) Summary The Metrologist I supports Analytical laboratories by performing routine calibration and instrument performance verification, maintenance and repairs on instrumentation including, but not limited to: High Pressure Liquid Chromatography/Ultra Performance Liquid Chromatography (HPLC/UPLC), ultra-violet visible spectrophotometry (UV-Vis), Fourier Transform Infrared (FTIR), Muffle Furnace, Viscometers, Density Meters, Melting Point, Dissolution and Autosampler, Polarimeter etc. following analytical methods, United States Pharmacopeia (USP)/National Formulary (NF) Chapters, protocols, Standard Operating Procedures (SOPs) under current Good Manufacturing Practices (cGMPs) and company policies. Collaborating closely with, and under the direct supervision of laboratory management, the incumbent carries out laboratory work to support laboratory activities and performs special projects as assigned. She/he also writes and assists investigation related to instrument calibration failures or other instrument related issues. ESSENTIAL FUNCTIONS Primary duties/responsibilities Carries out responsibilities in accordance with company policies, SOPs and state, federal and local laws Performs routine calibration and instrument performance verification, maintenance, and repairs on instrumentation such as HPLC/UPLC, UV-Vis, FTIR, Muffle Furnace, Viscometers, Density Meters, Melting Point, Dissolution and Autosampler, Polarimeter etc.; Performs routine daily calibration/verification checks for balances, pH meters, etc. Processes and reports calibration results using instrument specific data processing software; Documents all activities in legible manner following established formats and good documentation procedures Initiates, writes and assists investigation related to instrument calibration failures or other instrument related issues Contacts and obtains technical information from vendors or service providers Safely and properly dispose of chemical waste, as needed Complies with all company policies and procedures, including safety rules and regulations Adheres to cGMPs and current Good Documentation Practices (cGDPs) Requirements Requirements KNOWLEDGE/SKILLS/ABILITIES REQUIRED Minimum education and years of relevant work experience For Metrologist I - Bachelors in Chemistry, Engineering or related scientific field and 0-3 years lab experience in a GMP related industry or minimum 2 years related experience handling analytical equipment in pharmaceutical or biotechnology industry working in Metrology, Method Validation (MV), Quality Control (QC) or related laboratories. Special knowledge or skills needed and/or licenses or certificates required: Experience working with Food and Drug Administration (FDA), current Good Laboratory Practices (cGLPs), cGMPs, SOPs and regulatory rules, regulations, and guidelines Ability to follow procedures as written and report any discrepancies Proficiency with Microsoft Office Verbal and written communication and skills Ability to work independently and collaboratively, as required, in a fast paced, matrixed, team environment consisting of internal and external team members Analytical thinking with problem-solving skills and the ability to adapt to changing priorities and deadlines Planning, organization and time management skills including the ability to support and prioritize multiple projects Fluent in English (verbal and written) Ability to identify and distinguish colors Ability and willingness to work additional hours required by business needs Special knowledge or skills needed and/or licenses or certificates preferred: Experience performing or assisting in laboratory or metrology investigations Experience working in laboratories supporting testing of multiple dosage forms of products (i.e., solid dosage forms, liquid dosage forms, suspensions, etc.) Proficiency with Empower and/or other laboratory software Travel requirements: 0% Physical requirements: Laboratory based position Ability to lift up to 30 lbs Ability to use Personal Protective Equipment (PPE) Ability to stand for extended periods of time Anticipated salary range: Base salary offered is contingent on assessment of candidate’s education and experience level relative to requirements of the position and a review of related industry standards and internal equity. Additional benefits: In addition to base salary, full-time employees are also eligible for incentives, including, but not limited to: bonus eligible, medical, dental, vision, Rx insurance, 401K with match, life insurance, paid Company Holidays, PTO, Paid Volunteer Time and Employee Resource Groups. Tris Pharma, Inc. offers a highly competitive compensation and benefits package. To build and enhance our diverse workforce, we encourage applications from individuals with disabilities, minorities, veterans, women, LGBTQ, etc. Tris Pharma, Inc. is an Equal Opportunity Employer. #LI-_

Responsibilities

The Metrologist I supports Analytical laboratories by performing routine calibration and instrument performance verification, maintenance, and repairs on various instrumentation. The role involves documenting calibration results, assisting in investigations related to instrument issues, and ensuring compliance with company policies and regulations.