QC Sampling Associate

NOTICE: The posting is for local applicants only and is not for those applying for a global assignment or employees working outside of Cipla's U.S. Subsidiaries or Affiliates.

Job Title: QC Sampling Associate

FLSA Classification: Full-Time, Non-Exempt/Hourly Professional

Work Location: Central Islip, NY

Work Hours: General Shift: 9:00 AM – 5:30 PM (may vary based on business needs)

Reports To: Quality Control Director

Hourly Rate: $18.72 - $26.00

• Perform sample withdrawal for all incoming raw materials, packing materials including but not limited to receipt, logging distribution and destruction.
• Update all sample information in SAP as per company procedures.
• Complete data entry as required.
• Oversee temperature and humidity monitoring for retention and sample storage rooms.
• Conduct sample loading in stability chambers and submit stability samples as per schedule.
• Sampling of materials received at Invagen Warehouse locations for laboratory testing purposes as per the established sampling procedures.
• Assist in the shipment of the samples to contract labs as required.
• Provide general housekeeping in the QC lab and any other functional activity as assigned by management.
• Maintain and update the retention rooms of raw materials as required.
• Other duties as assigned.

• Minimum of High School Diploma or equivalent education credential (ex. GED) required.
• Proficient user of Microsoft Office Programs to include Word, Excel, Outlook, PowerPoint, and other lab-related systems.
• 2 years’ work experience in pharmaceutical, nutraceutical, or cosmetics raw materials sampling activity.
• Associate’s degree or higher in Chemistry, Laboratory Science, or related fields from an accredited institution (preferred).
• Proficiently speak English as a first or second language.
• Have excellent organization, learning and teaching skills required to work in teams.
• Ability to understand and analyze complex data.
• Working knowledge of Microsoft Office programs and other scientific‑based software.
• Experience in oral solid dosage is a plus.

• Hourly position.
• Full-time.
• Must be willing to work in a pharmaceutical packaging setting.
• Must be willing and able to work any assigned shift ranging from first or second shift.
• Work schedule may be Monday to Friday.
• Must be willing to work some weekends based on business needs as required by management.
• Must possess a positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors.
• No remote work available.
• No employment sponsorship or work visas.

This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required (e.g., uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection). Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work‑shift basis, where required (Day, Evening, Night).

Weekend or Holiday work may be requested or required. The position requires long periods of standing/walking, ability to ascend/descend ladders, and ability to lift up to 35 pounds.

Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

Salary/Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.