QC Analyst (I/II/III) – A Shift (Mon-Fri, 8am-5pm)

Evergreen Theragnostics; Springfield (NJ); On-site; USD 55,000 - 75,000; Full time

Job summary

Evergreen Theragnostics, a leading radiopharmaceutical company, is seeking a QC Analyst 1 for routine quality control testing. The ideal candidate will ensure compliance with industry standards and work hands-on with analytical instruments while maintaining safety protocols in a state-of-the-art laboratory facility.

Benefits

Medical insurance

Vision insurance

401(k)

Disability insurance

Paid maternity leave

Paid paternity leave

Qualifications

• Entry-level position with less than 2 years experience.
• Experience with laboratory instrumentation such as GC, TLC, HPLC.
• Willingness to follow strict safety protocols while handling hazardous materials.

Responsibilities

• Perform quality control testing of radiopharmaceutical products.
• Ensure compliance with internal SOPs and pharmaceutical regulations.
• Maintain a clean and safe laboratory environment.

Skills

Proficiency in Microsoft Office Suite

Strong communication skills

Detail-oriented

Ability to follow GMP and GDP requirements

Education

Bachelor’s degree in a scientific field

Tools

GC

TLC

HPLC

Job description

QC Analyst (I/II/III) – A Shift (Mon-Fri, 8am-5pm)

QC Analyst (I/II/III) – A Shift (Mon-Fri, 8am-5pm)

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Vice President Human Resources | Senior Human Resources Professional

About Us

Evergreen Theragnostics, Inc. is a radiopharmaceutical company headquartered in Springfield, NJ. We operate in a brand-new state-of-the-art facility, providing contract development and manufacturing services for radiopharmaceutical companies, including therapeutics and centrally distributed diagnostics. We also operate our own cutting edge cancer research laboratories, developing proprietary, radiotherapeutic medicines.

Evergreen is a small team, where all team members support each other in a variety of activities. We are looking for team members who are motivated to take on new challenges and join us as we start on our new journey as part of Lantheus.

QC Analyst 1

Job Title: QC Analyst 1 – Radiopharmaceuticals

Job Summary: The QC Analyst 1 is an entry-level position responsible for performing routine quality control testing of radiopharmaceutical products in accordance with industry standards, including Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). This role involves hands-on testing with scientific instrumentation, maintaining a safe and compliant laboratory environment, and ensuring that all radiopharmaceutical products meet established quality standards for release.

Key Responsibilities:

• Perform routine quality control (QC) analytical tests (e.g., GC, TLC, HPLC) for the release of radiopharmaceutical batches.
• Ensure that all testing and lab activities are conducted in compliance with internal SOPs, GMP, GDP, and other relevant pharmaceutical regulations.
• Operate and maintain laboratory equipment, ensuring that instruments are properly calibrated and functioning within specifications.
• Accurately document and record all test results, ensuring compliance with regulatory and company standards.
• Maintain a clean, safe, and organized lab environment, adhering to all safety and pharmaceutical regulations, including radiation safety protocols.
• Perform daily lab tasks, including solution preparation, drug product analysis, and documentation of all testing.
• Maintain strict attention to detail while working with hazardous materials and ensure proper handling of radioactive substances as per safety guidelines.

Qualifications:

• Education: Bachelor’s degree in a scientific field (e.g., Chemistry, Biochemistry, Life Sciences) or relevant work experience.
• Experience:
• Less than 2 years of experience in the pharmaceutical or life sciences industry.
• Experience operating scientific laboratory instrumentation such as GC, TLC, HPLC, or similar equipment.
• Skills:
• Proficiency in Microsoft Office Suite (Word, Excel, etc.)
• Strong communication and organizational skills.
• Comfortable working with radiation and following all safety protocols.
• Ability to follow strict GMP and GDP requirements.
• Additional Requirements:
• Ability to handle multiple projects (typically 1-5 internal projects).
• A proactive approach to ensuring a clean and compliant lab environment.
• Detail-oriented with the ability to document results and manage records in accordance with regulatory standards.

Working Conditions:

• Laboratory setting with exposure to radiation and other chemical hazards.
• Required to wear personal protective equipment (PPE) such as lab coats, gloves, and safety goggles.
• Ability to stand for extended periods and occasionally lift up to 25 pounds.

QC Analyst 2

Job Title: Quality Control Laboratory Analyst 2 – Radiopharmaceuticals

Job Description:

We are seeking a highly motivated and detail-oriented Quality Control Laboratory Analyst 2 to join our team. This individual will play a key role in ensuring the highest standards of quality and compliance in our radiopharmaceutical release processes. The ideal candidate will have a background in pharmaceutical or life sciences, and hands-on experience with analytical techniques such as GC (Gas Chromatography), TLC (Thin Layer Chromatography), and HPLC (High-Performance Liquid Chromatography).

Key Responsibilities:

• Perform quality control testing and analysis release testing of radiopharmaceutical products to ensure compliance with internal and external specifications and regulatory standards.
• Independently operate and maintain laboratory equipment, ensuring calibration and proper functionality.
• Maintain a clean, safe, and organized lab environment, adhering to all safety and pharmaceutical regulations, including radiation safety protocols.
• Perform daily lab tasks, including solution preparation, drug product analysis, and documentation of all testing.
• Utilize laboratory techniques including GC, TLC, and HPLC to perform a variety of testing procedures.
• Maintain thorough and accurate documentation of testing activities, results, and reports in accordance with SOPs (Standard Operating Procedures).
• Train and mentor new team members, offering support and guidance to ensure smooth onboarding and integration into laboratory operations.
• Maintain strict attention to detail while working with hazardous materials and ensure proper handling of radioactive substances as per safety guidelines.

Qualifications:

• 2-5 years of experience in the pharmaceutical, life sciences, or radiopharmaceutical industry
• Bachelor's degree in a scientific field (e.g., Chemistry, Biochemistry, Pharmaceutical Sciences), or equivalent relevant work experience.
• Proficiency and hands-on experience with laboratory techniques such as GC, TLC, and HPLC.
• Ability to work independently and as part of a team, managing multiple tasks and priorities.
• Strong problem-solving skills and attention to detail, with an understanding of GMP, GLP, and other regulatory requirements.
• Previous experience in training or mentoring new staff members is a plus.
• Laboratory setting with exposure to radiation and other chemical hazards.
• Required to wear personal protective equipment (PPE) such as lab coats, gloves, and safety goggles.
• Fast-paced laboratory setting with occasional lifting and movement of materials.
• Commitment to maintaining a clean, organized, and safe working environment.

QC Analyst 3

Job Title: Quality Control Laboratory Analyst 3 – Radiopharmaceuticals

Job Description:

We are looking for an experienced and proactive Quality Control Laboratory Analyst 3 to join our team. In this role, the candidate will participate in critical quality control processes for our radiopharmaceutical products, ensuring all operations comply with stringent industry standards and regulatory guidelines. The ideal candidate will have significant experience in pharmaceutical or radiopharmaceutical environments, a strong background in analytical techniques, and the ability to troubleshoot laboratory equipment.

Key Responsibilities:

• Lead quality control testing and analysis of radiopharmaceutical products, ensuring adherence to both internal specifications and regulatory standards.
• Maintain a clean, safe, and organized lab environment, adhering to all safety and pharmaceutical regulations, including radiation safety protocols.
• Perform daily lab tasks, including solution preparation, drug product analysis, and documentation of all testing.
• Independently operate, maintain, and troubleshoot laboratory equipment such as GC (Gas Chromatography), TLC (Thin Layer Chromatography), and HPLC (High-Performance Liquid Chromatography).
• Perform routine and complex analysis, troubleshooting issues with laboratory instrumentation as needed to ensure accurate results.
• Ability to be the primary QC operator on all projects, taking ownership of testing and analytical activities across multiple initiatives.
• Mentor and train new team members on laboratory techniques, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and company-specific procedures.
• Ensure proper documentation practices, maintaining a high level of accuracy in lab notebooks.
• Collaborate with cross-functional teams to resolve quality issues and contribute to continuous improvement initiatives.
• Assist with management of QC materials, including ordering supplies, tracking inventory, and ensuring availability of materials necessary for testing.

Qualifications:

• 5+ years of experience in the pharmaceutical, life sciences, or radiopharmaceutical industry
• Bachelor's degree in a scientific field (e.g., Chemistry, Biochemistry, Pharmaceutical Sciences), or equivalent relevant work experience.
• Extensive hands-on experience with laboratory techniques, including GC, TLC, and HPLC, as well as troubleshooting of each.
• Proven ability to be the primary QC analyst on complex projects, managing multiple responsibilities and ensuring quality deliverables.
• Strong experience in inventory management, including the ordering and monitoring of QC supplies and reagents.
• In-depth knowledge of GMP, GDP, and regulatory documentation standards.
• Strong troubleshooting and problem-solving skills related to laboratory equipment and procedures.
• Ability to mentor and train new team members on both technical skills and regulatory requirements, with a focus on GMP/GDP.
• Capable of maintaining detailed and accurate documentation in lab notebooks, with minimal QA corrections.
• Laboratory setting with exposure to radiation and other chemical hazards.
• Required to wear personal protective equipment (PPE) such as lab coats, gloves, and safety goggles.
• Fast-paced laboratory setting, requiring multitasking and prioritizing several projects.
• Occasional lifting and movement of materials; commitment to maintaining a safe and organized working environment.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Disability insurance

Paid maternity leave

Paid paternity leave

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