Chemist II

Curia • Albuquerque, NM

15h • Onsite

About The Position

Chemist II in Albuquerque, NM

Build your future at Curia, where our work has the power to save lives

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.

We proudly offer

Generous benefit options (eligible first day of employment)
Paid training, vacation and holidays (vacation accrual begins on first day of employment)
Career advancement opportunities
Education reimbursement
401K program with matching contributions
Learning platform
And more!

Summary:
The Chemist II performs routine and moderately complex analytical testing to support pharmaceutical manufacturing operations and customer requirements. This role independently conducts testing of raw materials, in-process materials, finished products, stability samples, plant water, and particulate samples using validated analytical methods and laboratory instrumentation. The Chemist II analyzes and interprets test results, identifies and investigates atypical findings, executes laboratory protocols, and prepares accurate technical documentation in accordance with current Good Manufacturing Practices (cGMP), data integrity requirements, and applicable regulatory standards. Responsibilities include supporting method transfers, new product implementation, laboratory investigations, equipment qualification, calibration, and maintenance activities, as well as reviewing laboratory documentation for accuracy and completeness. The Chemist II contributes to SOP revisions, assists with continuous improvement initiatives, collaborates with cross-functional teams to resolve technical issues, and serves as a technical resource to less experienced laboratory personnel. This role maintains audit readiness, performs work in accordance with aseptic gowning requirements, and complies with applicable DEA regulations, where required.

Requirements

• Bachelor’s degree in in Science, Chemistry, Biology or related field of study
• Minimum of three (3) year experience in chemistry or related role
• Ability to read and interpret various documents, such as safety instructions, standard operating procedures, technical procedures, and governmental regulations.
• Strong written and verbal communication skills, along with effective presentation skills.
• Proficient in executing arithmetic operations including addition, subtraction, multiplication, and division across various units of measurement, employing whole numbers, fractions, decimals, and percentages.
• Strong grasp of algebraic and geometric principles.
• Ability to define problems, collect data, establish facts, and draw valid conclusions.
• Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
• Strong technical foundation and proven capability in effectively utilizing diverse software tools to streamline the organization's daily functions.
• Adeptness in manufacturing and internet software, alongside proficiency in Microsoft Office tools including PowerPoint, Excel, Word, and Outlook.
• Leads with integrity and respect
• Demonstrates business acumen
• Champions change
• Promotes a safe and healthy work environment by actively identifying and addressing potential hazards, following established safety protocols, participating in safety training programs, and fostering a culture of awareness and responsibility among team members.
• Demonstrates strong attention to detail
• Proficient in the use of operational theories of all common laboratory equipment.
• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
• Ability to perform independent work related to projects and/or routine activities.
• Ability to meet deadlines and work under pressure with limited supervision.
• Ability to work effectively under pressure to meet deadlines.
• Be accessible to laboratory and plant area(s) and office staff and to use required office equipment.
• Must pass a background check
• Must pass a drug screen
• May be required to pass Occupational Health Screening

Nice To Haves

• Minimum of two (2) years experience of aseptic/sterile experience in a pharmaceutical or related industry, preferred
• Provides guidance, coaching, and mentorship to team members
• Fosters a collaborative and positive work environment
• Coaches and Develops

Responsibilities

• Independently perform routine and moderately complex analytical testing of raw materials, in-process samples, finished products, stability samples, plant water, and particulate samples in accordance with approved procedures, validated methods, and regulatory requirements.
• Operate, troubleshoot, and maintain standard laboratory instrumentation, including balances, pipettes, pH meters, UV/Visible spectrophotometers, Total Organic Carbon (TOC) analyzers, and other applicable analytical equipment.
• Accurately document laboratory activities, test results, observations, and conclusions in accordance with Good Documentation Practices (GDP), data integrity requirements, and applicable quality standards.
• Execute analytical protocols, prepare technical reports, complete data summaries, and support method transfers, new product onboarding activities, and laboratory implementation projects.
• Analyze and interpret analytical data, identify trends or atypical results, support basic laboratory investigations, and apply root cause analysis and risk assessment tools to assist with problem resolution.
• Review laboratory documentation, analytical data, and test results for accuracy, completeness, and compliance with established procedures.
• Enter and maintain analytical data within applicable laboratory data management systems and perform data review activities, including basic tracking and trending of results.
• Participate in the development, review, and revision of standard operating procedures (SOPs), ensuring alignment with current laboratory practices, regulatory expectations, and quality requirements.
• Train and provide guidance to less experienced laboratory personnel on analytical methods, equipment operation, procedures, and laboratory practices as needed.
• Participate in internal and external training programs to maintain technical knowledge, regulatory awareness, and proficiency in laboratory techniques and quality systems.
• Prepare laboratory supplies, equipment, and documentation required to support manufacturing activities and analytical testing operations.
• Assist with the qualification, evaluation, and implementation of new laboratory equipment, analytical procedures, and process improvements.
• Maintain laboratory equipment, organization, housekeeping, and audit readiness in accordance with Good Laboratory Practices (GLP), cGMP requirements, and company standards.
• Collaborate with manufacturing, quality, and other cross-functional teams to support testing requirements, resolve technical issues, and meet production schedules.
• Maintain proficiency in aseptic gowning procedures and comply with requirements for entry into aseptic processing areas.
• Maintain required DEA clearance and comply with applicable requirements for handling controlled substances, where applicable.
• Adhere to all safety, regulatory, quality, and company policies to ensure a compliant and safe working environment.
• Read/interpret SOPs to ensure compliance
• Maintain up to date trainings
• Other duties as assigned

Benefits

• Generous benefit options (eligible first day of employment)
• Paid training, vacation and holidays (vacation accrual begins on first day of employment)
• Career advancement opportunities
• Education reimbursement
• 401K program with matching contributions
• Learning platform

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level