Expired

Scientist II Analytical


USA
Permanent
USD90000 - USD120000
R and D
PR/532462_1738954595
Scientist II Analytical

Summary:

Join this innovative team and fast growing Biotech dedicated to advancing pharmaceutical research and development. Seeking a motivated and skilled Scientist with experience developing analytical methods for small molecule drug products to contribute to 2025 milestones.

Key Responsibilities:

  • Conduct laboratory activities & lead projects with minimal supervision, including analyzing raw materials, in-process materials, and finished pharmaceutical products for quality, safety, purity, strength, and identity.
  • Independently set up and operate lab equipment, prepare reagents, solvents, and solutions for analytical and formulation activities.
  • Maintain accurate records in lab notebooks and process analytical data using lab equipment such as HPLC/UPLC.
  • Support the manufacture of small molecule drug products and prepare samples for blend uniformity.
  • Perform equipment qualification and calibrations as directed.
  • Execute approved method transfer protocols.
  • Assist in training other scientists and perform additional tasks as assigned.
  • Participate in project activities, support project timelines, and contribute to team objectives.
  • Establish and maintain effective relationships with team members.
  • Conduct lab work in accordance with SOPs & STPs, following corporate safety rules and procedures.
  • Comply with all corporate guidelines and policies.

Qualifications:

  • Masters in Chemistry, Pharmacy, or related fields with at least 6-8 years of industry experience, or Ph.D. with 2-3 years of experience in the Pharmaceutical industry.
  • Proven ability and/or experience with compendial test methods or pharmaceutical manufacturing equipment.
  • Understanding of pharmaceutical equipment and computerized systems for operation and troubleshooting.
  • Specific experience with analytical and/or process equipment used in laboratories such as HPLC, IR/FTIR, UV-Vis AA, powder blender, etc.
  • Experience with Empower software
  • Knowledge and understanding of FDA cGMP requirements as they apply to the pharmaceutical industry.
  • Effective English written and oral communication skills, with the ability to write short technical documents such as memos, laboratory investigations, protocols, and reports.

FAQs

Congratulations, we understand that taking the time to apply is a big step. When you apply, your details go directly to the consultant who is sourcing talent. Due to demand, we may not get back to all applicants that have applied. However, we always keep your CV and details on file so when we see similar roles or see skillsets that drive growth in organisations, we will always reach out to discuss opportunities.

Yes. Even if this role isn’t a perfect match, applying allows us to understand your expertise and ambitions, ensuring you're on our radar for the right opportunity when it arises.

We also work in several ways, firstly we advertise our roles available on our site, however, often due to confidentiality we may not post all. We also work with clients who are more focused on skills and understanding what is required to future-proof their business. 

That's why we recommend registering your CV so you can be considered for roles that have yet to be created. 

Yes, we help with CV and interview preparation. From customised support on how to optimise your CV to interview preparation and compensation negotiations, we advocate for you throughout your next career move.