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Career Opportunities: QC Chemist II (88410)

unlimited holidays
Remote: 
Full Remote
Salary: 
70 - 90K yearly
Experience: 
Mid-level (2-5 years)
Work from: 
New York (USA), United States

Offer summary

Qualifications:

Bachelor's degree in physical sciences preferred., 3 years of Pharmaceutical QC lab experience., Understanding of lab equipment and QC techniques., Proficiency in English, both written and spoken..

Key responsabilities:

  • Perform testing of samples in QC laboratory.
  • Ensure compliance with cGMP practices and documentation.
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Cipla Pharmaceuticals XLarge http://www.cipla.com/
10001 Employees
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Job description

 

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.

 

Job Title

QC Chemist II

Organization Name

InvaGen Pharmaceuticals

Location

550 South Research Place Central Islip, NY 11722

7 Oser Ave, Hauppauge, NY 11788

Employment Type

(Hourly/ Full Time)

Full Time – Salaried/Exempt

Salary Range

(Base/ Hourly)

$70,000 - $90,000

Benefits

 In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance – medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) – vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid and unpaid family leave, employee discounts, and other benefits

Work Hours/ Shift/ Remote

8:30 AM – 5:00 PM

Responsibilities/ Accountabilities

The job of the "Chemist" is simple described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience or a combination of all three.

The general duties and responsibilities of the "Chemist" include but are not limited to the following:

  • Conduct routine testing or other analysis in a specific group or department setting.
  • Conduct advanced testing and/or critical testing, as required.
  • Operate specialized equipment or conduct specialized skill testing.
  • Participate in investigation activities.
  • Ensure compliance to all data integrity and cGMP practices, procedures, and expectations.
  • Ensure compliance with all god documentation practices.
  • Other duties and responsibilities as assigned by the Head of the Department.

Education Qualifications

  • Bachelor's degree (BS or BA), physical sciences preferred.
  • Masters or (MS) or Doctorate (PhD)
  • Proficiently speak English as a first or second language
  • Proficiently communicate and understand (read and write) scientific work in English.
  • 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

  • Must have a minimum of three (3) years of Pharmaceutical QC lab experience.
  • Must have a background within the Pharmaceutical industry.
  • Understanding of lab equipment and QC testing techniques required.

Skills/ Competencies

  • UV, HPLC, DSC, and other tests.
  • Know how to use dissolution instruments.
  • LIMS and Empower

Physical Requirements

  • Work standing or walking unassisted for 75% or greater of an 8-hour period.
  • Unassisted lifting up-to 10 kg, may be required.
  • Able to wear appropriate personal protective equipment at all times, when required.
  • Sitting at a desk and/or working at a computer or other “screen” 75% or greater of an 8-hour period.

Other Information

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.

No remote work available. Relocation available.

 

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.

 

Equal Opportunity Employer

 

Cipla USA & its U.S. Affiliates are committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.


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 a reasonable accommodation to make your application or interview experience a great one, please contact careers.northamerica@cipla.com.

 

Pre-employment Process

 

Applicants who receive a conditional offer must satisfactory complete pre-employment drug testing.

 

Disclaimer on Pay Ranges

 

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 and company results.

 

 

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Teaching
  • Teamwork
  • Lifelong Learning

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