Manufacturing Associate I - 2nd Shift

Par Health

Village of Hobart (NY)

On-site

USD 26,640 - 37,941

Full time

14 days+
Application generator

Get a reply from this employer — a resume and cover letter tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

Par Health is seeking a Manufacturing Associate at its Hobart, NY facility. In this role, you will process compound materials into final tablet form while adhering to strict cGMP guidelines and ensuring quality control. The position requires attention to detail and the ability to follow instructions effectively.

You will also manage production processes, conduct equipment inspections, and maintain accurate documentation. Starting pay is $23.44 per hour plus a $2.00 shift differential with opportunities for bonuses.

Qualifications

  • Basic knowledge of mathematical concepts and English grammar.
  • Recommended 3 to 12 months of experience in a manufacturing environment.

Responsibilities

  • Processes compound materials into tablet form and conducts quality checks.
  • Maintains compliance with cGMP and safety guidelines.
  • Operates equipment required for manufacturing pharmaceuticals.

Skills

Attention to detail
Ability to follow instructions
Basic mathematical skills

Education

High school diploma or GED

Job description

Why Us?

At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With a global workforce, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.

Job Description Summary

Processes active compound materials into final tablet form performing quality control checks to maintain consistency of product according to manufacturing specifications. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate is expected to fully participate in both departmental projects and any quality working teams that may be applicable. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and compliant documentation on all activities.

Job Description
Raw Materials and Equipment Checklist Successfully Completed

Obtain and weigh in products for all shifts. Moves raw materials and product to/from vault, cage, process or storage areas. Inspects machine parts for unusual wear and proper lubrication. Operates equipment required in the manufacture of pharmaceutical product. Performs/reviews quality checks on weight, thickness, hardness and friability of tablets at various stages of the process according to manufacturing instructions and SOPs. Submits product samples to quality laboratories as required. Maintains product batch, room activity, and equipment records. Maintains control of DEA scheduled material in accordance with accepted policy, practice and procedure.

Work Center Schedule and Shift Attainment Achieved to Standards

Is at his/her position on the line ready to start production as required. Monitors the production process, makes periodic checks and adjusts equipment or work practices to maximize production efficiency, yields, quality and safety. Accurately reports production and ensures reports are completed as required.

Operator Responsibilities
  • Performs operator-level machine adjustments and lubrication. Assists technicians with minor machine repairs and set-up. Troubleshoots problems with equipment and processing to assist other technicians to minimize disruptions to production.
  • Ensures that line conditions are acceptable to change from one product to another by ensuring that materials, paperwork, and equipment have been staged for changeover.
Downtime Avoided

Will immediately stop manufacturing and notify Line Leader of any safety or quality concerns. Documents inspections performed and keeps accurate equipment records, clean-up sheets and other required paperwork. Disassembles, cleans and reassembles basic line equipment according to SOPs. Insures proper inspections are conducted prior to reassembly. Cleans and assembles dust collector. Assists in the training of individuals on equipment and processes in the department.

Compliance Standards Met

Follows all EHS rules and regulations. Accepts accountability for own personal safety and identifies potential unsafe conditions to help prevent self and co-workers from being injured. Complies with all site security requirements. Performs lock‑out/tag‑out procedures according to SOPs. Follows safe working practices in the execution of their assigned duties. Collects all process related hazardous wastes and transports to accumulation drums. Actively participates in general site and departmental Safety initiatives. Maintains clean work area; clear away debris, damaged or defective product, cartons, labels and packaging supplies.

Escalation Process Adhered to

Makes initial attempts to identify root cause within scope of decision‑making authority while simultaneously notifying next level of leadership. If attempts at the next level do not resolve the problem and the Associate believes that a higher level needs to be involved, the problem is escalated to the highest level.

Marginal Functions

Assists technicians at other stations within the department as needed. Works on any tableting stations on which you are trained. May be cross‑trained in other functions.

Minimum Requirements
Education

Requires a high school diploma or GED. Basic knowledge and ability to apply mathematical concepts, spelling, reading English, and grammar.

Experience

Recommended minimum of three to twelve months’ experience under direct supervision and guidance in order to gain sufficient skill to perform the requirements of the position.

License(s)/Certification(s) Required

None required.

Working Conditions
Physical/Visual Activities or Demands
  • Heavy physical demand requires frequent moving, pushing, pulling, rolling and dumping of up to 100 kg and manual lifting of up to 25 kg. Physical demand also involves walking and standing (70%), balancing, bending, kneeling and reaching (15%), grasping and feeling (5%) and communicating (10%).
  • Mental demand is frequent requiring attention to details of specific manufacturing instructions and recording of information on paperwork.
  • Visual demand is continuous and requires clarity of vision at 20 inches or less and 20 feet or more with peripheral vision and the ability to bring objects into sharp focus, to judge distance and space relationships and to identify and distinguish colors.
Environmental/Atmospheric Conditions
  • Exposure to pure raw materials requires incumbent to wear a respirator on a regular basis.
  • Protective clothing and equipment including uniform shirt and slacks, jacket, safety glasses, booties, hairnet, gloves, disposable respirator, hearing protection, PAPR, and tyvek suit are worn continuously in the performance of the job functions.
  • Exposure to noise requires incumbent to wear hearing protection on regular basis.
  • Work hazards include proximity to moving mechanical parts, exposure to dust, odors, cleaning agents, noise, and vibration.
Location and Hours

Location: Hobart, NY Facility. Hours: Monday – Thursday 4:00pm to 2:15am. Must have the ability to work overtime when needed.

Pay Transparency

Expected base pay: $23.44 per hour plus a $2.00 shift differential. This position is eligible for a bonus in accordance with the terms of the applicable program. Bonuses are awarded at the Company's discretion. This position is not eligible for visa sponsorship. Applicants must be authorized to work in the United States without current or future sponsorship needs.

EEO Statement

We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provide equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Manufacturing Associate I - 3rd Shift
Manufacturing Associate I - 3rd Shift

Par Health • Village of Hobart (NY)

On-site
USD 31,000 - 44,000
Bonus eligibility
High Volume Plant Technician- 2nd shift
High Volume Plant Technician- 2nd shift

Paladin Labs Inc. • Village of Hobart (NY)

On-site
USD 41,000 - 44,000
Bonus program
High Volume Plant Technician- 2nd shift
High Volume Plant Technician- 2nd shift

Paladin Labs Inc. • New York (NY)

On-site
USD 60,000 - 68,000
Blending Technician I 3rd Shift Mon - Thurs 8:00pm - 6:15am
Blending Technician I 3rd Shift Mon - Thurs 8:00pm - 6:15am

Par Health • Village of Hobart (NY)

On-site
USD 48,000 - 54,000
Blending Technician I 2nd Shift Mon - Thurs 4:00pm - 2:15am
Blending Technician I 2nd Shift Mon - Thurs 4:00pm - 2:15am

Paladin Labs Inc. • New York (NY), Northern (KY)

On-site
USD 67,502,000 - 71,635,000
Pharmaceutical Operator I
Pharmaceutical Operator I

Par Health • North Carolina

On-site
USD 43,000 - 61,000
Packaging Operator I - 1st Shift
Packaging Operator I - 1st Shift

Paladin Labs Inc. • New York (NY)

On-site
USD 31,684 - 34,440
Quality Assurance Tech II
Quality Assurance Tech II

Par Health • St. Louis (MO)

On-site
USD 52,000 - 76,000
Pharmaceutical Operator I
Pharmaceutical Operator I

Paladin Labs Inc. • Raleigh (NC)

On-site
USD 40,000 - 65,000
Pharmaceutical Operator 1
Pharmaceutical Operator 1

Paladin Labs Inc. • Raleigh (NC), Northern (KY)

On-site
USD 25,000 - 36,000