Claims Correspond Qc Analyst Jobs

Sample registration and entry in LIMS.

Location: Madhurantakam - Quality Control

Company: Sun Pharmaceutical Industries Ltd

2 - 5 years of experience preferred, or equivalent level of skill and experience.

Previous experience with microbiology assays and aseptic techniques in a GMP manufacturing environment is preferred.

Hands-on experience with one or more microbiology techniques: membrane filtration, inoculation (broth/agar), serial dilutions, biochemical tests, microbial identification, enumeration, environmental monitoring.

Require good written and verbal communication skills, good team work skills

Computer skills (MS Office, MS Project) or comparable word-processing and spreadsheet applications is required.

Bachelor or Master Degree in an applied science (microbiology preferred).

Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice

Manage and prioritize workload to meet deadlines

Examine all early pay submission forms

Certify all early and overnight payments have been processed correctly

Establish new accounts by importing data

Coordinate with other teams to resolve early payment issues

Completes other duties as assigned by Laboratory Management and/or Group Lead.

Demonstrates a working knowledge of the LIMS computer system. Enters data and

Laboratory experience is a plus.

Good practical knowledge of the laboratory environment.

Maintains accurate, complete, legible, and concurrent records of work performed and

Enters results in the laboratory notebook.

Knowledge of cGMP, Quality Systems, and ICH / regulatory guidance.

Alternatively, Master’s degree in above areas with 1 year of experience in a pharmaceutical/biotech QC laboratory or PhD in above areas.

Analytical testing to support product in-process, release, and stability programs.

Conduct, compile, and/or review Out of Specification lab investigations, deviations, and corrective and preventative actions plans.

Work with cross-functional teams to advance projects, maintain equipment, and authoring of documents and reports.

A commitment to Kashiv’s Vision, Mission, and Values is essential.

Maintains all training requirements for assigned tasks

Adhere to QMS policy and regulatory requirements.

EHS Responsibilities – All Associates

Quality Responsibilities – All Associates

We are looking for professionals with these required skills to achieve our goals:

programs as part of the offering.

Other Knowledge, Skills, and Abilities:

Responsible for communicating atypical and out-of-specification results to laboratory management.

Works with supervisor to prioritize activities. Shifts prioritizes to meet business demands. Notifies management when timelines cannot be met.

pharmaceutical industry and with analytical chemistry knowledge. Experience working in a

Demonstrates an understanding of the applicable test methods and a familiarity with compendial testing requirements.

Works independently or in a team setting with minimal supervision. Is accountable for the completion of individual responsibilities.

Excellent project management and organizational skills, with attention to detail

Implements and manages appropriate QC systems for data compliance and data management

Proven knowledge in cGMP raw material program (RM sampling plans and testing requirements)

Supports raw material qualification program by ensuring proper documentation of raw material qualification testing status

Develops and reviews non-compendial method qualification protocols and reports

Excellent oral and written communication skills. Ability to communicate professionally with vendors, internal customers and sales professionals regarding quality issues

Perform data entry and peer review for accuracy in accordance with laboratory procedures.

Knowledge of basic laboratory practices required and QC testing methods preferred.

Experience with Sanger sequencing method preferred.

The essential requirements of the job include:

Independently perform sequencing assay according to established standard operating procedures, including primer design, plate set-up, and sequencing result analysis

Use Codon Code Aligner, Snap Gene, and Primer Premier software to complete daily tasks

Pay: $26/hr on w2 (without benefits)

Typical related responsibilities will include but are not limited to the following:

Remote Position but local Miami candidates are preferred if there is an on-site need.

Bachelor’s degree in field with 0-2 years exp. Quality or Service. related IT, Audit, Field Engineer, Biomed.

Uses existing procedures to solve standard problems; analyses information and standard practices to make judgments.

Experience working with radiopharmaceuticals will be considered an asset but is not a requirement

Adhering to all applicable procedures, cGLP, cGMPs, company policies and any other quality or regulatory requirements.

BS or BA in STEM with a minimum of one year of relevant industry experience in analytical laboratories.

Experience working in a pharmaceutical GMP manufacturing environment is preferred

Work with radioactive materials using safe protocols to maintain ALARA principles.

Maintaining accurate and complete lab data documentation as per cGLP and/or cGMP, as appropriate.

Skilled in multi-tasking and adapting to changing business requirements in a dynamic corporate environment;

Bachelor's degree in Biochemistry or Chemistry with 4+ years of industry experience, or equivalent combination of education and experience;

Experience with a cGMP and global regulatory compliance organization;

Strong computer and communication skills;

Experience with equipment and analytical and/or biological method validation laboratory execution;

Ability to learn and perform tests and experiments, perform accurate data entry and keep information organized;

REMOTE - Work From Home Opportunity !

o Assist with resolving claims quality issues by identifying, documenting, and communicating with management.

o 2 years’ experience working with healthcare claims, medical billing, or authorization data

o Experience with researching and resolving escalated claims issues

o Knowledge of claims functions including working understanding of claims payments and denials

o Experience with IBM Dynamics (TriWest 360 CRM) or other CRM applications

We offer an excellent benefit package, including:

Working knowledge of Empower software and the creation of methods and custom fields

Experience with USP interpretation and testing

Support QC audit readiness with understanding of FDA and ISO regulations and requirements

Employ sound and compliant laboratory techniques and logic per industry standards (e.g., FDA, USP/NF, ISO, ANSI) and internal and customer requirements

Any additional functions as assigned by the Laboratory Manager

Knowledge, skills, and expertise in performing chemical experiments that involve the use of liquids, or "wet" chemicals.

Strong understanding of the underlying principles of chemistry, as well as knowledge of laboratory safety and best practices

Hands on analytical instrumentation experience is preferred.

Strong verbal and written communication skills

Strategic thinker with strong analytical skills who can translate client needs into actionable value-added projects/results.

Curious and adaptable – can transform knowledge into actionable activities.

Min Knowledge & Experience Required for the Position:

Maintains documentation of all work performed in accordance with GMP requirements.

Performs automated and manual assays as detailed in departmental/plant SOP's and QC Monographs, including raw material, in-process and finished product.

Interprets test results against specifications and decides if assays pass or fail.

Performs product stability, proficiency and environmental testing (Orangeburg).

Responsible for routine preventive maintenance, general troubleshooting, general cleanliness and calibration of Lab equipment

Enters final results and raw data for tested materials or products in LIMS (Laboratory Information Management System) as needed.

Bachelor’s degree in a science field with knowledge and experience in one of the following areas: Chemistry, Biology, or Microbiology

Full-Time Health Benefits on Your First Day

1-3 years of laboratory experience in related field

Wet chemistry experience preferred (ex. Acid/Base Titrations, water content)

Must have applied working knowledge of various laboratory instrumentation

Management of periodic reviews of analytical test procedures and SOPs as required

Technical training and mentorship of lesser experienced chemistry personnel

4+ years' experience in a quality role within the pharmaceutical industry

Experience in cGMP testing/manufacturing environments

Working knowledge of Empower 3

Strong technical knowledge of bio-analytical and chemistry analytical techniques

REMOTE - Work From Home Opportunity !

o Assist with resolving claims quality issues by identifying, documenting, and communicating with management.

o 2 years’ experience working with healthcare claims, medical billing, or authorization data

o Experience with researching and resolving escalated claims issues

o Experience with Claims Systems

o Experience in interpreting policies, monitoring compliance, and developing processes