Scientist: Synthetic Molecule Analytical Chemistry

ThermoFisher Scientific; South San Francisco (CA); On-site; USD 45,000 - 51,000; Full time

Benefits offered by this job

Healthcare

Annual incentive plan bonus

Employee assistance program

Commuter benefits

Tuition reimbursement

Paid time off (PTO)

Employee stock purchase plan (ESPP)

Job summary

Thermo Fisher Scientific is seeking a Scientist to perform routine to complex sample analysis in a fully onsite role at South SF, CA. You will develop methods, troubleshoot instruments, and ensure data quality in GMP/GLP compliant workflows.

The candidate should hold a Bachelor's in lab sciences and have 2–4 years’ relevant experience, with proficiency in LC-MS/HPLC techniques and strong data documentation skills. This position offers a competitive benefits package and on-site work in California.

Qualifications

• Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Biology or related field.
• Experience in analytical methods and regulatory guidelines (GMP/GLP).
• Ability to document experiments clearly and communicate progress.

Responsibilities

• Perform routine to complex sample preparation and analysis for pharma/biopharma compounds.
• Develop analytical methods and troubleshoot instruments as needed.
• Review data against SOPs and product specifications, preparing reports.
• Train others on instrument operation and GMP/GLP compliance.
• Communicate project status to the project leader and collaborators.

Skills

Data analysis

Documentation

Communication

GMP/GLP knowledge

Excel proficiency

Time management

Education

Bachelor's degree in lab sciences

Tools

HPLC-UV

HPLC-CAD

LC-MS

PSD

ELN

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

This is a fully onsite role based at our customer’s site in South SF, CA. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.

Must be legally authorized to work in the United States withoutsponsorship.

Must be able to pass a comprehensive background check, whichincludes a drug screening.

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.

Our Laboratories Functional Service Partnership (FSP) team plays a direct role in advancing drug development by creating sustained groups of talent within our customers’ organizations to provide long-term support. Through this collaborative approach, our professionals bring their commitment to excellence, industry knowledge, and operational strength directly into customer environments, helping to enhance capabilities and advance the delivery of life-changing therapies.

Key responsibilities:

Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications.

• Perform routine analysis for drug substances, drug products, intermediates as well as starting materials

• Perform analytical method development and instrument/method troubleshooting as necessary

• Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing.

• Problem solves with assistance pertaining to extraction and/or instrumentation problems.

• Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.

• Manages QC/QA responsibilities without supervisor or QA input.

• Communicates project status to project leader.

• Performs work assignments accurately, and in a timely and safe manner.

• Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices(GMP) or Good Laboratory Practices (GLP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.

Education and Experience:

• Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar

• Scientist: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2-4 years’)

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

• Independently perform analysis using different techniques, including HPLC-UV, HPLC-CAD, LC-MS, PSD

• Clearly document the experiment using ELN and proactively communicate progress with project lead and collaborators

• Be comfortable to present the work to the team

• Knowledge of applicable regulatory authority, compendia and ICH guidelines

• Ability to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation and instrument use

• Ability to utilize Microsoft Excel and Word to perform tasks

• Ability to independently optimize analytical methods

• Good written and oral communication skills

• Time management and project management skills

• Problem solving and troubleshooting abilities

• Ability to work in a collaborative work environment with a team

Working Environment:

Below is listed the working environment/requirements for this role:

Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.

Able to work upright and stationary and/or standing for typical working hours.

Able to lift and move objects up to 25 pounds

Able to work in non-traditional work environments.

Able to use and learn standard office equipment and technology with proficiency.

May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.

Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Compensation and Benefits

The hourly pay range estimated for this position based in California is $32.89–$37.20.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

• A choice of national medical and dental plans, and a national vision plan, including health incentive programs

• Employee assistance and family support programs, including commuter benefits and tuition reimbursement

• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

• Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.