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Analytical Scientist III

Company: Bevov
Location: Raleigh
Posted on: October 15, 2021

Job Description:

Job Description

Our client is a world-class contract development and manufacturing organization. They are a team of dynamic individuals committed to developing life-saving drugs around the world.  A mindset of innovation, accountability, and customer focus inspires us to be the most efficient, safe, and reliable choice for their customers and the patients they serve.  In return, they offer challenging careers, accelerated professional growth, and the opportunity to be part of something different.

The Associate Scientist III is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing.

The Associate Scientist may also be required to work on method development/method validation projects. For this position, HPLC and/or GC-based methodologies are commonly employed in the described testing.

Other key methodologies applied include titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). The position requires superior leadership behaviors of the company core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile.


  • Performs one or more of the following techniques: residual solvents, assays (potencies, related substances), elemental impurities, moisture content, identification, and various other wet chemistry-based measurements.
  • Evaluates and interpret generated data.
  • Analyses information for technical correctness and accuracy.
  • Understands the theoretical basis of methods/experiments.
  • Solves problems of diverse scope in which analysis of data requires evaluation of identifiable factors.
  • Writes test procedures, protocols, and reports.
  • Maintains working knowledge of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
  • Maintains a safe, clean, and organized work environment free of safety hazards.
  • Safely handles potent compounds
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.


  • Bachelor’s degree in Pharmaceutical Sciences, Chemistry or equivalent with 5 years of experience or Master’s degree with 3 years of experience required.
  • 2+ years of experience in Pharmaceutical, CDMO, or cGMP preferred.  
  • Consistently demonstrates honesty and integrity through personal example.
  • Follows all safety policies and leads by example a safety-first culture.
  • Produces high-quality work products with a focus on first time right.
  • Complies with the company code of conduct and policies and regulatory standards.
Core Leadership Competencies·        
  • Thinks strategically. Quickly identifies and acts on opportunities. Considers the downstream impact. Seeks to understand the why. Focuses on work that matters.
  • Develops organization and others. Takes ownership to develop self and others. Seeks out new opportunities and experiences for continuous learning.
  • Acts decisively. Makes and acts on decisions quickly. Makes decisions with the customer and their patients in mind. Meets commitments with a sense of urgency. Seeks ways to be more efficient.
  • Drives performance. Holds self and others accountable. Delivers results the first time right. Never settles for the status quo. Willing to have tough conversations. Asks for feedback and takes action to improve.
  • Passion for customers. Listens to understand. Asks the right questions. Gets to the heart of the matter and uses that insight to provide value.

    ·         Works collaboratively. Seeks out the experience of others with the aim for better results. Open-minded regardless of where ideas originate. Flexible and easy to work with.

Functional Competencies
  • Excellent verbal and written communication and documentation skills are required.
  • Excellent detail orientation and organizational skills are required.
  • Excellent problem-solving and basic troubleshooting ability required.
  • Excellent knowledge of Laboratory equipment and safety required.
  • Expert knowledge of Laboratory Documentation is required.
  • Working knowledge of cGMP in a pharmaceutical or regulated environment preferred.
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.    
Decision Making and Supervision Required
  • Applies job skills and company policies and SOPs to complete a broad range of difficult tasks.
  • Receives minimal instruction on day-to-day work, general instructions on new assignments. 
Travel Requirements: Up to 5% travel required.


Client Offer You:
Competitive salary with career advancement opportunities
Bonus plan
•    Medical, dental and vision coverage from day one
•    401(k) with company match
•    Company paid vacation, holiday and sick leave
•    Voluntary benefits including short & long-term disability, life, accident, critical illness insurances

Diversity and Inclusion:
  The client values diversity and we are committed to creating an inclusive environment for all employees.  All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, pregnancy, age, national origin, physical or mental disability, past or present military service, marital status, gender identification or expression, medical condition (including genetic characteristics) or any other protected characteristic as established by law.  

As part of our effort to provide and maintain a safe and healthful workplace, the Client requires new hires to be fully vaccinated against COVID-19.  Individuals are considered fully vaccinated 2 weeks after their second dose of the Pfizer or Moderna vaccine, or 2 weeks after a single dose of the Johnson & Johnson vaccine. Individuals seeking an exemption from this requirement for medical or religious reasons should contact HR to complete a request for accommodation form.

Keywords: Bevov, Raleigh , Analytical Scientist III, Other , Raleigh, North Carolina

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