Microbiologist, MSAT

Job Description

Job Description

At Argenta, we’re more than a company — we’re a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it.

Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market.

We’re in a unique position. We are the world’s only combined contract research and contract development and manufacturing organization (CRO/CDMO) dedicated to animal health.

Our uniqueness means:

We are ambitious, growing and building a ‘one team’ culture, guided by our values.

• • We are team players;
  • We are doers;
  • We are customer-centric;
  • We are innovators .

We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best “paw” forward we will make the lives of the animals we care for, better.

With bases in New Zealand, the US, the UK and Europe, our 900+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Let’s Make It Happen, Together.

TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply. 

Argenta is currently looking to fill the role of Microbiologist, MSAT   at our Shawnee, KS  location. This position leads the preparation of protocols and execution of cGMP microbiological method development/feasibility, transfer, verification/suitability, and validation of active ingredient, raw material, cleaning verification, and finished drug product analysis.  Position manages multiple concurrent projects and has client interface responsibility with client counterparts and project teams.  The position requires analyzing in-process, raw materials and finished product of pharmaceuticals for quality, safety, purity, strength and identity by conducting analysis as specified in the applicable specification requirements following GLP and cGMP guidelines.  Position will support setup and qualification of new instrumentation and equipment in the laboratory as required.

Key Responsibilities:

• Performs and maintains accurate, detailed records for method development/optimization, method transfer/suitability/validation, and for routine analysis of finished pharmaceutical dosages and/or raw materials following approved analytical methodology and specifications to pharmaceutical cGMP requirements.
• Independently manages the Design and execution of method transfer and/ or suitability protocols, method validations and reports.
• Lead the activities to develop microbiological methods to assess the purity, potency, other key attributes, and stability of drug substances and finished products performing testing including sterility, endotoxin, bioburden/microbial limits, ELISA, sub visible particulate, and microbial identifications. Dosage forms including sterile injectables, solid oral dose, soft chews, and non-sterile liquids and pastes.
• Responsible in ensuring testing is in adherence to schedules through team-oriented process. Manages effectively own assigned workload and develops timelines for assigned projects to provide to management.
• Reads and interprets USP, EP, JP compendial monographs, and other guidance sources of methodology.
• Serve as a subject matter expert in advanced laboratory practices by writing SOP’s.
• Utilizes root cause analysis tools and technical writing to independently complete laboratory investigations.
  
• Provides technical subject matter expert input and addresses work performed on project calls both with internal project teams and to external clients.

About You:

• Bachelor’s degree in biology or related Science field with work experience in cGMP and/or GLP chemistry lab environment (a minimum of 3 years of work experience with B.S. or 1 year of work experience with masters (M.S) is preferred).
• Proficient at performing microbiological testing techniques including sterility, endotoxin, bioburden/microbial limits, ELISA, sub visible particulate, gram stains, and microbial identifications.  Testing of dosage forms including liquid and solid raw materials/API, sterile injectables, solid oral dose, soft chews, and non-sterile liquids and pastes.
• Proficiency with operating equipment and instruments including sterility testing isolators and decontamination system, endotoxin instrumentation, ELISA instrumentation, sub-visible particulate instrumentation, laminar flow hoods, autoclaves, balances, pH meters, and microbial identification instruments.
• Knowledge of pharmaceutical aseptic processes and requirements preferred.
• Ability to effectively manage multiple projects to meet committed scope, cost, and schedule.
• Strong technical writing to independently author protocols, test methods, procedures, investigations/deviations, and technical papers which may be submitted to regulatory authorities.
• Knowledge of GMP and FDA manufacturing regulations
• Ability to analyze and interpret data
• Strong written and oral communication skills

Argenta has strongly embedded company values which is key to who we are and how we deliver. We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued.  At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through a strong culture, great benefits, and growth opportunities.

Argenta is an equal-opportunity employer

To find out more about Argenta, click here: