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QC Lab Technician I
QC Lab Technician ICipla • Central Islip, NY, United States
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QC Lab Technician I

QC Lab Technician I

Cipla • Central Islip, NY, United States
[job_card.30_days_ago]
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  • [job_card.full_time]
[job_card.job_description]

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

Job Title : Quality Control (QC) Lab Technician

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 : $16.64 - $22.88

Purpose :

The content and statements documented in this job description are designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent of this job description is to be representative of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position satisfactorily and in accordance with the established performance expectations.

Scope :

The scope (content and statements) of this job description is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role.

Duties and Responsibilities

The general duties and responsibilities of the Quality Control Lab Technician include but are not limited to

the following :

  • Perform sample management for all incoming raw materials, in-process, finished products and stability samples including but not limited to receipt, logging distribution and destruction.
  • Coordinate chemical and reference standard inventory in the lab, verifying the expired chemicals and standards and discarding as per company procedures.
  • Update all sample information in SAP as per company procedures.
  • Complete data entry as required.
  • Maintain lab consumables supply and placing orders as per requirement
  • Oversee temperature and humidity monitoring for stability chambers
  • Conduct sample loading in stability chambers and submitting stability samples as per schedule.
  • 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.
  • Other duties as assigned.

Education and Experience :

  • 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 a laboratory setting.
  • Associates degree or higher in Chemistry, Laboratory Science, or related fields of study from an accredited institution. (Preferred)
  • Bachelor's degree (BS or BA), physical sciences 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 sets.
  • Working knowledge of Microsoft Office programs and other scientific based software.
  • Experience in oral solid dosage is a plus.
  • Professional and Behavioral Competencies

  • 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.
  • Working conditions

    This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. 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.Long periods of standing up / walking during the working hours; ability to ascent / decent ladders; and able to lift up to 35 pounds.

    About Cipla

    Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.

    Driven by the purpose 'Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

    In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division.

    InvaGen Pharmaceuticals, Inc.

    InvaGen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States.

    Equal Opportunity Employer

    Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

    At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter.

    About the 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.

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